Canonical Allele Identifier: CA388675044
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875627A>C , CM000675.2:g.102875627A>C GRCh38
NC_000013.10:g.103527977A>C , CM000675.1:g.103527977A>C GRCh37
NC_000013.9:g.102325978A>C NCBI36
NG_007146.1:g.34804A>C , LRG_464:g.34804A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4386A>C (ERCC5)
ENST00000682869.1:n.3934A>C (ERCC5)
ENST00000683246.1:n.4922A>C (ERCC5)
ENST00000683642.1:n.3515A>C (ERCC5)
ENST00000639132.1:c.3960A>C (BIVM-ERCC5) ENSP00000492684.1:p.Glu1320Asp
ENST00000639435.1:c.4647A>C (BIVM-ERCC5) ENSP00000491742.1:p.Glu1549Asp
ENST00000651002.1:c.*3046A>C (ERCC5) ENSP00000498809.1:n.*3046A>C
ENST00000651055.1:n.3412A>C (ERCC5)
ENST00000651281.1:n.3653A>C (ERCC5)
ENST00000651387.1:n.2769A>C (ERCC5)
ENST00000651470.1:c.*457A>C (ERCC5) ENSP00000498701.1:n.*457A>C
ENST00000652225.2:c.3285A>C (ERCC5) MANE Select ENSP00000498881.2:p.Glu1095Asp
ENST00000652613.1:c.2781A>C (ERCC5) ENSP00000498357.1:p.Glu927Asp
ENST00000355739.8:c.3285A>C (ERCC5) ENSP00000347978.4:p.Glu1095Asp
ENST00000375954.1:c.984A>C (ERCC5) ENSP00000365121.1:p.Glu328Asp
ENST00000472247.1:n.445A>C (ERCC5)
ENST00000610537.4:c.3282A>C (ERCC5) ENSP00000478667.1:p.Glu1094Asp
NM_000123.3:c.3285A>C , LRG_464t1:c.3285A>C (ERCC5) NP_000114.2:p.Glu1095Asp
NM_001204425.1:c.4647A>C (BIVM-ERCC5) NP_001191354.1:p.Glu1549Asp
NM_000123.4:c.3285A>C (ERCC5) MANE Select NP_000114.3:p.Glu1095Asp
NM_001204425.2:c.4647A>C (BIVM-ERCC5) NP_001191354.2:p.Glu1549Asp