Canonical Allele Identifier: CA2115211027

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102862923G= , CM000675.2:g.102862923G=	GRCh38
NC_000013.10:g.103515273G= , CM000675.1:g.103515273G=	GRCh37
NC_000013.9:g.102313274G=	NCBI36
NG_007146.1:g.22100G= , LRG_464:g.22100G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.2015G= (ERCC5)
ENST00000682869.1:n.2423G= (ERCC5)
ENST00000683246.1:n.2551G= (ERCC5)
ENST00000639132.1:c.2449G= (BIVM-ERCC5)	ENSP00000492684.1:p.Val817=
ENST00000639435.1:c.3136G= (BIVM-ERCC5)	ENSP00000491742.1:p.Val1046=
ENST00000651002.1:c.*1535G= (ERCC5)	ENSP00000498809.1:n.*1535G=
ENST00000651055.1:n.1903G= (ERCC5)
ENST00000651281.1:n.2142G= (ERCC5)
ENST00000651387.1:n.1258G= (ERCC5)
ENST00000651470.1:c.1774G= (ERCC5)	ENSP00000498701.1:p.Val592=
ENST00000652225.2:c.1774G= (ERCC5) MANE Select	ENSP00000498881.2:p.Val592=
ENST00000652613.1:c.1270G= (ERCC5)	ENSP00000498357.1:p.Val424=
ENST00000355739.8:c.1774G= (ERCC5)	ENSP00000347978.4:p.Val592=
ENST00000602836.1:c.3050G= (BIVM-ERCC5)
ENST00000610537.4:c.1774G= (ERCC5)	ENSP00000478667.1:p.Val592=
NM_000123.3:c.1774G= , LRG_464t1:c.1774G= (ERCC5)	NP_000114.2:p.Val592=
NM_001204425.1:c.3136G= (BIVM-ERCC5)	NP_001191354.1:p.Val1046=
NM_000123.4:c.1774G= (ERCC5) MANE Select	NP_000114.3:p.Val592=
NM_001204425.2:c.3136G= (BIVM-ERCC5)	NP_001191354.2:p.Val1046=