Canonical Allele Identifier: CA655556212
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

COSMIC: COSN214322

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873217T>A , CM000675.2:g.102873217T>A GRCh38
NC_000013.10:g.103525567T>A , CM000675.1:g.103525567T>A GRCh37
NC_000013.9:g.102323568T>A NCBI36
NG_007146.1:g.32394T>A , LRG_464:g.32394T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.3939T>A (ERCC5)
ENST00000682869.1:n.3529-42T>A (ERCC5)
ENST00000683246.1:n.4475T>A (ERCC5)
ENST00000683642.1:n.3068T>A (ERCC5)
ENST00000639132.1:c.3555-42T>A (BIVM-ERCC5) ENSP00000492684.1:n.3555-42T>A
ENST00000639435.1:c.4242-42T>A (BIVM-ERCC5) ENSP00000491742.1:n.4242-42T>A
ENST00000651002.1:c.*2641-42T>A (ERCC5) ENSP00000498809.1:n.*2641-42T>A
ENST00000651055.1:n.3009-44T>A (ERCC5)
ENST00000651281.1:n.3248-42T>A (ERCC5)
ENST00000651387.1:n.2364-42T>A (ERCC5)
ENST00000651470.1:c.*52-42T>A (ERCC5) ENSP00000498701.1:n.*52-42T>A
ENST00000652225.2:c.2880-42T>A (ERCC5) MANE Select ENSP00000498881.2:n.2880-42T>A
ENST00000652613.1:c.2376-42T>A (ERCC5) ENSP00000498357.1:n.2376-42T>A
ENST00000355739.8:c.2880-42T>A (ERCC5) ENSP00000347978.4:n.2880-42T>A
ENST00000375954.1:c.579-42T>A (ERCC5) ENSP00000365121.1:n.579-42T>A
ENST00000610537.4:c.2877-42T>A (ERCC5) ENSP00000478667.1:n.2877-42T>A
NM_000123.3:c.2880-42T>A , LRG_464t1:c.2880-42T>A (ERCC5) NP_000114.2:n.2880-42T>A
NM_001204425.1:c.4242-42T>A (BIVM-ERCC5) NP_001191354.1:n.4242-42T>A
NM_000123.4:c.2880-42T>A (ERCC5) MANE Select NP_000114.3:n.2880-42T>A
NM_001204425.2:c.4242-42T>A (BIVM-ERCC5) NP_001191354.2:n.4242-42T>A