Canonical Allele Identifier: CA2115215332

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873279G= , CM000675.2:g.102873279G=	GRCh38
NC_000013.10:g.103525629G= , CM000675.1:g.103525629G=	GRCh37
NC_000013.9:g.102323630G=	NCBI36
NG_007146.1:g.32456G= , LRG_464:g.32456G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4001G= (ERCC5)
ENST00000682869.1:n.3549G= (ERCC5)
ENST00000683246.1:n.4537G= (ERCC5)
ENST00000683642.1:n.3130G= (ERCC5)
ENST00000639132.1:c.3575G= (BIVM-ERCC5)	ENSP00000492684.1:p.Gly1192=
ENST00000639435.1:c.4262G= (BIVM-ERCC5)	ENSP00000491742.1:p.Gly1421=
ENST00000651002.1:c.*2661G= (ERCC5)	ENSP00000498809.1:n.*2661G=
ENST00000651055.1:n.3027G= (ERCC5)
ENST00000651281.1:n.3268G= (ERCC5)
ENST00000651387.1:n.2384G= (ERCC5)
ENST00000651470.1:c.*72G= (ERCC5)	ENSP00000498701.1:n.*72G=
ENST00000652225.2:c.2900G= (ERCC5) MANE Select	ENSP00000498881.2:p.Gly967=
ENST00000652613.1:c.2396G= (ERCC5)	ENSP00000498357.1:p.Gly799=
ENST00000355739.8:c.2900G= (ERCC5)	ENSP00000347978.4:p.Gly967=
ENST00000375954.1:c.599G= (ERCC5)	ENSP00000365121.1:p.Gly200=
ENST00000610537.4:c.2897G= (ERCC5)	ENSP00000478667.1:p.Gly966=
NM_000123.3:c.2900G= , LRG_464t1:c.2900G= (ERCC5)	NP_000114.2:p.Gly967=
NM_001204425.1:c.4262G= (BIVM-ERCC5)	NP_001191354.1:p.Gly1421=
NM_000123.4:c.2900G= (ERCC5) MANE Select	NP_000114.3:p.Gly967=
NM_001204425.2:c.4262G= (BIVM-ERCC5)	NP_001191354.2:p.Gly1421=