Canonical Allele Identifier: CA388569316
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102856083G>C , CM000675.2:g.102856083G>C GRCh38
NC_000013.10:g.103508433G>C , CM000675.1:g.103508433G>C GRCh37
NC_000013.9:g.102306434G>C NCBI36
NG_007146.1:g.15260G>C , LRG_464:g.15260G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.740G>C (ERCC5)
ENST00000682869.1:n.1148G>C (ERCC5)
ENST00000683246.1:n.1276G>C (ERCC5)
ENST00000684184.1:n.1145G>C (ERCC5)
ENST00000638434.1:c.597G>C (BIVM-ERCC5)
ENST00000639132.1:c.1174G>C (BIVM-ERCC5) ENSP00000492684.1:p.Glu392Gln
ENST00000639435.1:c.1861G>C (BIVM-ERCC5) ENSP00000491742.1:p.Glu621Gln
ENST00000651002.1:c.*260G>C (ERCC5) ENSP00000498809.1:n.*260G>C
ENST00000651055.1:n.628G>C (ERCC5)
ENST00000651281.1:n.867G>C (ERCC5)
ENST00000651470.1:c.499G>C (ERCC5) ENSP00000498701.1:p.Glu167Gln
ENST00000652225.2:c.499G>C (ERCC5) MANE Select ENSP00000498881.2:p.Glu167Gln
ENST00000652613.1:c.-6G>C (ERCC5) ENSP00000498357.1:n.-6G>C
ENST00000355739.8:c.499G>C (ERCC5) ENSP00000347978.4:p.Glu167Gln
ENST00000535557.5:c.499G>C (ERCC5) ENSP00000442117.1:p.Glu167Gln
ENST00000602836.1:c.1775G>C (BIVM-ERCC5)
ENST00000610537.4:c.499G>C (ERCC5) ENSP00000478667.1:p.Glu167Gln
NM_000123.3:c.499G>C , LRG_464t1:c.499G>C (ERCC5) NP_000114.2:p.Glu167Gln
NM_001204425.1:c.1861G>C (BIVM-ERCC5) NP_001191354.1:p.Glu621Gln
NM_000123.4:c.499G>C (ERCC5) MANE Select NP_000114.3:p.Glu167Gln
NM_001204425.2:c.1861G>C (BIVM-ERCC5) NP_001191354.2:p.Glu621Gln