Canonical Allele Identifier: CA2115216461
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875540G= , CM000675.2:g.102875540G= GRCh38
NC_000013.10:g.103527890G= , CM000675.1:g.103527890G= GRCh37
NC_000013.9:g.102325891G= NCBI36
NG_007146.1:g.34717G= , LRG_464:g.34717G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4299G= (ERCC5)
ENST00000682869.1:n.3847G= (ERCC5)
ENST00000683246.1:n.4835G= (ERCC5)
ENST00000683642.1:n.3428G= (ERCC5)
ENST00000639132.1:c.3873G= (BIVM-ERCC5) ENSP00000492684.1:p.Glu1291=
ENST00000639435.1:c.4560G= (BIVM-ERCC5) ENSP00000491742.1:p.Glu1520=
ENST00000651002.1:c.*2959G= (ERCC5) ENSP00000498809.1:n.*2959G=
ENST00000651055.1:n.3325G= (ERCC5)
ENST00000651281.1:n.3566G= (ERCC5)
ENST00000651387.1:n.2682G= (ERCC5)
ENST00000651470.1:c.*370G= (ERCC5) ENSP00000498701.1:n.*370G=
ENST00000652225.2:c.3198G= (ERCC5) MANE Select ENSP00000498881.2:p.Glu1066=
ENST00000652613.1:c.2694G= (ERCC5) ENSP00000498357.1:p.Glu898=
ENST00000355739.8:c.3198G= (ERCC5) ENSP00000347978.4:p.Glu1066=
ENST00000375954.1:c.897G= (ERCC5) ENSP00000365121.1:p.Glu299=
ENST00000472247.1:n.358G= (ERCC5)
ENST00000610537.4:c.3195G= (ERCC5) ENSP00000478667.1:p.Glu1065=
NM_000123.3:c.3198G= , LRG_464t1:c.3198G= (ERCC5) NP_000114.2:p.Glu1066=
NM_001204425.1:c.4560G= (BIVM-ERCC5) NP_001191354.1:p.Glu1520=
NM_000123.4:c.3198G= (ERCC5) MANE Select NP_000114.3:p.Glu1066=
NM_001204425.2:c.4560G= (BIVM-ERCC5) NP_001191354.2:p.Glu1520=