Canonical Allele Identifier: CA612112964

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs758731631
• gnomAD v2: 13-103525574-C-G
• gnomAD v4: 13-102873224-C-G
• MyVariant Identifiers: chr13:g.103525574C>G (hg19) ; chr13:g.102873224C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873224C>G , CM000675.2:g.102873224C>G	GRCh38
NC_000013.10:g.103525574C>G , CM000675.1:g.103525574C>G	GRCh37
NC_000013.9:g.102323575C>G	NCBI36
NG_007146.1:g.32401C>G , LRG_464:g.32401C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.3946C>G (ERCC5)
ENST00000682869.1:n.3529-35C>G (ERCC5)
ENST00000683246.1:n.4482C>G (ERCC5)
ENST00000683642.1:n.3075C>G (ERCC5)
ENST00000639132.1:c.3555-35C>G (BIVM-ERCC5)	ENSP00000492684.1:n.3555-35C>G
ENST00000639435.1:c.4242-35C>G (BIVM-ERCC5)	ENSP00000491742.1:n.4242-35C>G
ENST00000651002.1:c.*2641-35C>G (ERCC5)	ENSP00000498809.1:n.*2641-35C>G
ENST00000651055.1:n.3009-37C>G (ERCC5)
ENST00000651281.1:n.3248-35C>G (ERCC5)
ENST00000651387.1:n.2364-35C>G (ERCC5)
ENST00000651470.1:c.*52-35C>G (ERCC5)	ENSP00000498701.1:n.*52-35C>G
ENST00000652225.2:c.2880-35C>G (ERCC5) MANE Select	ENSP00000498881.2:n.2880-35C>G
ENST00000652613.1:c.2376-35C>G (ERCC5)	ENSP00000498357.1:n.2376-35C>G
ENST00000355739.8:c.2880-35C>G (ERCC5)	ENSP00000347978.4:n.2880-35C>G
ENST00000375954.1:c.579-35C>G (ERCC5)	ENSP00000365121.1:n.579-35C>G
ENST00000610537.4:c.2877-35C>G (ERCC5)	ENSP00000478667.1:n.2877-35C>G
NM_000123.3:c.2880-35C>G , LRG_464t1:c.2880-35C>G (ERCC5)	NP_000114.2:n.2880-35C>G
NM_001204425.1:c.4242-35C>G (BIVM-ERCC5)	NP_001191354.1:n.4242-35C>G
NM_000123.4:c.2880-35C>G (ERCC5) MANE Select	NP_000114.3:n.2880-35C>G
NM_001204425.2:c.4242-35C>G (BIVM-ERCC5)	NP_001191354.2:n.4242-35C>G