Canonical Allele Identifier: CA388675125
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875664T>A , CM000675.2:g.102875664T>A GRCh38
NC_000013.10:g.103528014T>A , CM000675.1:g.103528014T>A GRCh37
NC_000013.9:g.102326015T>A NCBI36
NG_007146.1:g.34841T>A , LRG_464:g.34841T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4423T>A (ERCC5)
ENST00000682869.1:n.3971T>A (ERCC5)
ENST00000683246.1:n.4959T>A (ERCC5)
ENST00000683642.1:n.3552T>A (ERCC5)
ENST00000639132.1:c.3997T>A (BIVM-ERCC5) ENSP00000492684.1:p.Ser1333Thr
ENST00000639435.1:c.4684T>A (BIVM-ERCC5) ENSP00000491742.1:p.Ser1562Thr
ENST00000651002.1:c.*3083T>A (ERCC5) ENSP00000498809.1:n.*3083T>A
ENST00000651055.1:n.3449T>A (ERCC5)
ENST00000651281.1:n.3690T>A (ERCC5)
ENST00000651387.1:n.2806T>A (ERCC5)
ENST00000651470.1:c.*494T>A (ERCC5) ENSP00000498701.1:n.*494T>A
ENST00000652225.2:c.3322T>A (ERCC5) MANE Select ENSP00000498881.2:p.Ser1108Thr
ENST00000652613.1:c.2818T>A (ERCC5) ENSP00000498357.1:p.Ser940Thr
ENST00000355739.8:c.3322T>A (ERCC5) ENSP00000347978.4:p.Ser1108Thr
ENST00000375954.1:c.1021T>A (ERCC5) ENSP00000365121.1:p.Ser341Thr
ENST00000472247.1:n.482T>A (ERCC5)
ENST00000610537.4:c.3319T>A (ERCC5) ENSP00000478667.1:p.Ser1107Thr
NM_000123.3:c.3322T>A , LRG_464t1:c.3322T>A (ERCC5) NP_000114.2:p.Ser1108Thr
NM_001204425.1:c.4684T>A (BIVM-ERCC5) NP_001191354.1:p.Ser1562Thr
NM_000123.4:c.3322T>A (ERCC5) MANE Select NP_000114.3:p.Ser1108Thr
NM_001204425.2:c.4684T>A (BIVM-ERCC5) NP_001191354.2:p.Ser1562Thr