Canonical Allele Identifier: CA2115210994
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102862847A= , CM000675.2:g.102862847A= GRCh38
NC_000013.10:g.103515197A= , CM000675.1:g.103515197A= GRCh37
NC_000013.9:g.102313198A= NCBI36
NG_007146.1:g.22024A= , LRG_464:g.22024A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.1939A= (ERCC5)
ENST00000682869.1:n.2347A= (ERCC5)
ENST00000683246.1:n.2475A= (ERCC5)
ENST00000639132.1:c.2373A= (BIVM-ERCC5) ENSP00000492684.1:p.Glu791=
ENST00000639435.1:c.3060A= (BIVM-ERCC5) ENSP00000491742.1:p.Glu1020=
ENST00000651002.1:c.*1459A= (ERCC5) ENSP00000498809.1:n.*1459A=
ENST00000651055.1:n.1827A= (ERCC5)
ENST00000651281.1:n.2066A= (ERCC5)
ENST00000651387.1:n.1182A= (ERCC5)
ENST00000651470.1:c.1698A= (ERCC5) ENSP00000498701.1:p.Glu566=
ENST00000652225.2:c.1698A= (ERCC5) MANE Select ENSP00000498881.2:p.Glu566=
ENST00000652613.1:c.1194A= (ERCC5) ENSP00000498357.1:p.Glu398=
ENST00000355739.8:c.1698A= (ERCC5) ENSP00000347978.4:p.Glu566=
ENST00000602836.1:c.2974A= (BIVM-ERCC5)
ENST00000610537.4:c.1698A= (ERCC5) ENSP00000478667.1:p.Glu566=
NM_000123.3:c.1698A= , LRG_464t1:c.1698A= (ERCC5) NP_000114.2:p.Glu566=
NM_001204425.1:c.3060A= (BIVM-ERCC5) NP_001191354.1:p.Glu1020=
NM_000123.4:c.1698A= (ERCC5) MANE Select NP_000114.3:p.Glu566=
NM_001204425.2:c.3060A= (BIVM-ERCC5) NP_001191354.2:p.Glu1020=