Canonical Allele Identifier: CA2115216476

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102875580G= , CM000675.2:g.102875580G=	GRCh38
NC_000013.10:g.103527930G= , CM000675.1:g.103527930G=	GRCh37
NC_000013.9:g.102325931G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000123.4:c.3238G= (ERCC5) MANE Select	NP_000114.3:p.Gly1080=
ENST00000652225.2:c.3238G= (ERCC5) MANE Select	ENSP00000498881.2:p.Gly1080=
NM_001204425.2:c.4600G= (BIVM-ERCC5)	NP_001191354.2:p.Gly1534=
ENST00000355739.8:c.3238G= (ERCC5)	ENSP00000347978.4:p.Gly1080=
ENST00000375954.1:c.937G= (ERCC5)	ENSP00000365121.1:p.Gly313=
ENST00000472247.1:n.398G= (ERCC5)
ENST00000610537.4:c.3235G= (ERCC5)	ENSP00000478667.1:p.Gly1079=
ENST00000639132.1:c.3913G= (BIVM-ERCC5)	ENSP00000492684.1:p.Gly1305=
ENST00000639435.1:c.4600G= (BIVM-ERCC5)	ENSP00000491742.1:p.Gly1534=
ENST00000651002.1:c.*2999G= (ERCC5)	ENSP00000498809.1:n.*2999G=
ENST00000651055.1:n.3365G= (ERCC5)
ENST00000651281.1:n.3606G= (ERCC5)
ENST00000651387.1:n.2722G= (ERCC5)
ENST00000651470.1:c.*410G= (ERCC5)	ENSP00000498701.1:n.*410G=
ENST00000652613.1:c.2734G= (ERCC5)	ENSP00000498357.1:p.Gly912=
ENST00000682632.1:n.4339G= (ERCC5)
ENST00000682869.1:n.3887G= (ERCC5)
ENST00000683246.1:n.4875G= (ERCC5)
ENST00000683642.1:n.3468G= (ERCC5)