Canonical Allele Identifier: CA255225480

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs761359775
• gnomAD v4: 13-102862848-A-G
• MyVariant Identifiers: chr13:g.103515198A>G (hg19) ; chr13:g.102862848A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102862848A>G , CM000675.2:g.102862848A>G	GRCh38
NC_000013.10:g.103515198A>G , CM000675.1:g.103515198A>G	GRCh37
NC_000013.9:g.102313199A>G	NCBI36
NG_007146.1:g.22025A>G , LRG_464:g.22025A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.1940A>G (ERCC5)
ENST00000682869.1:n.2348A>G (ERCC5)
ENST00000683246.1:n.2476A>G (ERCC5)
ENST00000639132.1:c.2374A>G (BIVM-ERCC5)	ENSP00000492684.1:p.Thr792Ala
ENST00000639435.1:c.3061A>G (BIVM-ERCC5)	ENSP00000491742.1:p.Thr1021Ala
ENST00000651002.1:c.*1460A>G (ERCC5)	ENSP00000498809.1:n.*1460A>G
ENST00000651055.1:n.1828A>G (ERCC5)
ENST00000651281.1:n.2067A>G (ERCC5)
ENST00000651387.1:n.1183A>G (ERCC5)
ENST00000651470.1:c.1699A>G (ERCC5)	ENSP00000498701.1:p.Thr567Ala
ENST00000652225.2:c.1699A>G (ERCC5) MANE Select	ENSP00000498881.2:p.Thr567Ala
ENST00000652613.1:c.1195A>G (ERCC5)	ENSP00000498357.1:p.Thr399Ala
ENST00000355739.8:c.1699A>G (ERCC5)	ENSP00000347978.4:p.Thr567Ala
ENST00000602836.1:c.2975A>G (BIVM-ERCC5)
ENST00000610537.4:c.1699A>G (ERCC5)	ENSP00000478667.1:p.Thr567Ala
NM_000123.3:c.1699A>G , LRG_464t1:c.1699A>G (ERCC5)	NP_000114.2:p.Thr567Ala
NM_001204425.1:c.3061A>G (BIVM-ERCC5)	NP_001191354.1:p.Thr1021Ala
NM_000123.4:c.1699A>G (ERCC5) MANE Select	NP_000114.3:p.Thr567Ala
NM_001204425.2:c.3061A>G (BIVM-ERCC5)	NP_001191354.2:p.Thr1021Ala