Canonical Allele Identifier: CA2115216513

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102875638G= , CM000675.2:g.102875638G=	GRCh38
NC_000013.10:g.103527988G= , CM000675.1:g.103527988G=	GRCh37
NC_000013.9:g.102325989G=	NCBI36
NG_007146.1:g.34815G= , LRG_464:g.34815G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4397G= (ERCC5)
ENST00000682869.1:n.3945G= (ERCC5)
ENST00000683246.1:n.4933G= (ERCC5)
ENST00000683642.1:n.3526G= (ERCC5)
ENST00000639132.1:c.3971G= (BIVM-ERCC5)	ENSP00000492684.1:p.Gly1324=
ENST00000639435.1:c.4658G= (BIVM-ERCC5)	ENSP00000491742.1:p.Gly1553=
ENST00000651002.1:c.*3057G= (ERCC5)	ENSP00000498809.1:n.*3057G=
ENST00000651055.1:n.3423G= (ERCC5)
ENST00000651281.1:n.3664G= (ERCC5)
ENST00000651387.1:n.2780G= (ERCC5)
ENST00000651470.1:c.*468G= (ERCC5)	ENSP00000498701.1:n.*468G=
ENST00000652225.2:c.3296G= (ERCC5) MANE Select	ENSP00000498881.2:p.Gly1099=
ENST00000652613.1:c.2792G= (ERCC5)	ENSP00000498357.1:p.Gly931=
ENST00000355739.8:c.3296G= (ERCC5)	ENSP00000347978.4:p.Gly1099=
ENST00000375954.1:c.995G= (ERCC5)	ENSP00000365121.1:p.Gly332=
ENST00000472247.1:n.456G= (ERCC5)
ENST00000610537.4:c.3293G= (ERCC5)	ENSP00000478667.1:p.Gly1098=
NM_000123.3:c.3296G= , LRG_464t1:c.3296G= (ERCC5)	NP_000114.2:p.Gly1099=
NM_001204425.1:c.4658G= (BIVM-ERCC5)	NP_001191354.1:p.Gly1553=
NM_000123.4:c.3296G= (ERCC5) MANE Select	NP_000114.3:p.Gly1099=
NM_001204425.2:c.4658G= (BIVM-ERCC5)	NP_001191354.2:p.Gly1553=