Canonical Allele Identifier: CA2115216488
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875599G= , CM000675.2:g.102875599G= GRCh38
NC_000013.10:g.103527949G= , CM000675.1:g.103527949G= GRCh37
NC_000013.9:g.102325950G= NCBI36
NG_007146.1:g.34776G= , LRG_464:g.34776G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4358G= (ERCC5)
ENST00000682869.1:n.3906G= (ERCC5)
ENST00000683246.1:n.4894G= (ERCC5)
ENST00000683642.1:n.3487G= (ERCC5)
ENST00000639132.1:c.3932G= (BIVM-ERCC5) ENSP00000492684.1:p.Gly1311=
ENST00000639435.1:c.4619G= (BIVM-ERCC5) ENSP00000491742.1:p.Gly1540=
ENST00000651002.1:c.*3018G= (ERCC5) ENSP00000498809.1:n.*3018G=
ENST00000651055.1:n.3384G= (ERCC5)
ENST00000651281.1:n.3625G= (ERCC5)
ENST00000651387.1:n.2741G= (ERCC5)
ENST00000651470.1:c.*429G= (ERCC5) ENSP00000498701.1:n.*429G=
ENST00000652225.2:c.3257G= (ERCC5) MANE Select ENSP00000498881.2:p.Gly1086=
ENST00000652613.1:c.2753G= (ERCC5) ENSP00000498357.1:p.Gly918=
ENST00000355739.8:c.3257G= (ERCC5) ENSP00000347978.4:p.Gly1086=
ENST00000375954.1:c.956G= (ERCC5) ENSP00000365121.1:p.Gly319=
ENST00000472247.1:n.417G= (ERCC5)
ENST00000610537.4:c.3254G= (ERCC5) ENSP00000478667.1:p.Gly1085=
NM_000123.3:c.3257G= , LRG_464t1:c.3257G= (ERCC5) NP_000114.2:p.Gly1086=
NM_001204425.1:c.4619G= (BIVM-ERCC5) NP_001191354.1:p.Gly1540=
NM_000123.4:c.3257G= (ERCC5) MANE Select NP_000114.3:p.Gly1086=
NM_001204425.2:c.4619G= (BIVM-ERCC5) NP_001191354.2:p.Gly1540=