Canonical Allele Identifier: CA2115211032

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102862938G= , CM000675.2:g.102862938G=	GRCh38
NC_000013.10:g.103515288G= , CM000675.1:g.103515288G=	GRCh37
NC_000013.9:g.102313289G=	NCBI36
NG_007146.1:g.22115G= , LRG_464:g.22115G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.2030G= (ERCC5)
ENST00000682869.1:n.2438G= (ERCC5)
ENST00000683246.1:n.2566G= (ERCC5)
ENST00000639132.1:c.2464G= (BIVM-ERCC5)	ENSP00000492684.1:p.Val822=
ENST00000639435.1:c.3151G= (BIVM-ERCC5)	ENSP00000491742.1:p.Val1051=
ENST00000651002.1:c.*1550G= (ERCC5)	ENSP00000498809.1:n.*1550G=
ENST00000651055.1:n.1918G= (ERCC5)
ENST00000651281.1:n.2157G= (ERCC5)
ENST00000651387.1:n.1273G= (ERCC5)
ENST00000651470.1:c.1789G= (ERCC5)	ENSP00000498701.1:p.Val597=
ENST00000652225.2:c.1789G= (ERCC5) MANE Select	ENSP00000498881.2:p.Val597=
ENST00000652613.1:c.1285G= (ERCC5)	ENSP00000498357.1:p.Val429=
ENST00000355739.8:c.1789G= (ERCC5)	ENSP00000347978.4:p.Val597=
ENST00000602836.1:c.3065G= (BIVM-ERCC5)
ENST00000610537.4:c.1789G= (ERCC5)	ENSP00000478667.1:p.Val597=
NM_000123.3:c.1789G= , LRG_464t1:c.1789G= (ERCC5)	NP_000114.2:p.Val597=
NM_001204425.1:c.3151G= (BIVM-ERCC5)	NP_001191354.1:p.Val1051=
NM_000123.4:c.1789G= (ERCC5) MANE Select	NP_000114.3:p.Val597=
NM_001204425.2:c.3151G= (BIVM-ERCC5)	NP_001191354.2:p.Val1051=