CALCA

Calcitonin related polypeptide alpha P01258 CALC_HUMAN
Protein Coding Chr 11 11p15.2 Swiss-Prot reviewed Entrez 796
Mutations
244
CL 44 · Tissue 198
Samples
115
CL 24 · Tissue 90
Peptides
110
unique mutant peptides
Transcripts
3
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations24444198
Samples1152490
Peptides1102192

Function

CALCA · Calcitonin related polypeptide alpha

This gene encodes the peptide hormones calcitonin, calcitonin gene-related peptide and katacalcin by tissue-specific alternative RNA splicing of the gene transcripts and cleavage of inactive precursor proteins. Calcitonin is involved in calcium regulation and acts to regulate phosphorus metabolism. Calcitonin gene-related peptide functions as a vasodilator and as an antimicrobial peptide while katacalcin is a calcium-lowering peptide. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2014].

Isoforms & Proteins

3 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000331587 P01258 92 77
ENST00000396372 P01258 81 72
ENST00000486207 P06881 71 65

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11p15.2
Entrez ID
Aliases
CALC1CGRPCGRP-ICGRP-alphaCGRP1CT

Recurrent Mutations

All 77 amino-acid changes on canonical ENST00000331587 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in CALCA · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in CALCA – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
4/40 10%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Squamous Cell Lung Carcinoma
0/57 0%
8/810 1%
Non-Small Cell Lung Carcinoma
3/304 1%
12/1390 1%
Other Solid Cancers
0/94 0%
11/1515 1%
Gastric Carcinoma
2/74 3%
8/1809 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Burkitts Lymphoma
1/32 3%
0/196 0%
Mesothelioma
1/62 2%
0/165 0%
Melanoma
0/210 0%
9/1899 0%
Head and Neck Carcinoma
1/85 1%
6/1574 0%
Colorectal Carcinoma
1/143 1%
10/3239 0%
Endometrial Carcinoma
0/42 0%
2/612 0%
Esophageal Squamous Cell Carcinoma
4/51 8%
4/2550 0%
Biliary Tract Carcinoma
1/54 2%
2/950 0%
Glioma
0/52 0%
5/2127 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
4/2534 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Carcinoma
1/23 4%
0/769 0%
Breast Carcinoma
0/144 0%
3/3264 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%
Other Blood Cancers
1/61 2%
0/2725 0%

Mutation Distribution

Where CALCA is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CALCA were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 46 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 244 mutations in CALCA

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide