Canonical Allele Identifier: CA388674860
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4299G>C (ERCC5)
ENST00000682869.1:n.3847G>C (ERCC5)
ENST00000683246.1:n.4835G>C (ERCC5)
ENST00000683642.1:n.3428G>C (ERCC5)
ENST00000639132.1:c.3873G>C (BIVM-ERCC5) ENSP00000492684.1:p.Glu1291Asp
ENST00000639435.1:c.4560G>C (BIVM-ERCC5) ENSP00000491742.1:p.Glu1520Asp
ENST00000651002.1:c.*2959G>C (ERCC5) ENSP00000498809.1:n.*2959G>C
ENST00000651055.1:n.3325G>C (ERCC5)
ENST00000651281.1:n.3566G>C (ERCC5)
ENST00000651387.1:n.2682G>C (ERCC5)
ENST00000651470.1:c.*370G>C (ERCC5) ENSP00000498701.1:n.*370G>C
ENST00000652225.2:c.3198G>C (ERCC5) MANE Select ENSP00000498881.2:p.Glu1066Asp
ENST00000652613.1:c.2694G>C (ERCC5) ENSP00000498357.1:p.Glu898Asp
ENST00000355739.8:c.3198G>C (ERCC5) ENSP00000347978.4:p.Glu1066Asp
ENST00000375954.1:c.897G>C (ERCC5) ENSP00000365121.1:p.Glu299Asp
ENST00000472247.1:n.358G>C (ERCC5)
ENST00000610537.4:c.3195G>C (ERCC5) ENSP00000478667.1:p.Glu1065Asp
NM_000123.3:c.3198G>C , LRG_464t1:c.3198G>C (ERCC5) NP_000114.2:p.Glu1066Asp
NM_001204425.1:c.4560G>C (BIVM-ERCC5) NP_001191354.1:p.Glu1520Asp
NM_000123.4:c.3198G>C (ERCC5) MANE Select NP_000114.3:p.Glu1066Asp
NM_001204425.2:c.4560G>C (BIVM-ERCC5) NP_001191354.2:p.Glu1520Asp