Canonical Allele Identifier: CA388673530
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873301T>A , CM000675.2:g.102873301T>A GRCh38
NC_000013.10:g.103525651T>A , CM000675.1:g.103525651T>A GRCh37
NC_000013.9:g.102323652T>A NCBI36
NG_007146.1:g.32478T>A , LRG_464:g.32478T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4023T>A (ERCC5)
ENST00000682869.1:n.3571T>A (ERCC5)
ENST00000683246.1:n.4559T>A (ERCC5)
ENST00000683642.1:n.3152T>A (ERCC5)
ENST00000639132.1:c.3597T>A (BIVM-ERCC5) ENSP00000492684.1:p.Asp1199Glu
ENST00000639435.1:c.4284T>A (BIVM-ERCC5) ENSP00000491742.1:p.Asp1428Glu
ENST00000651002.1:c.*2683T>A (ERCC5) ENSP00000498809.1:n.*2683T>A
ENST00000651055.1:n.3049T>A (ERCC5)
ENST00000651281.1:n.3290T>A (ERCC5)
ENST00000651387.1:n.2406T>A (ERCC5)
ENST00000651470.1:c.*94T>A (ERCC5) ENSP00000498701.1:n.*94T>A
ENST00000652225.2:c.2922T>A (ERCC5) MANE Select ENSP00000498881.2:p.Asp974Glu
ENST00000652613.1:c.2418T>A (ERCC5) ENSP00000498357.1:p.Asp806Glu
ENST00000355739.8:c.2922T>A (ERCC5) ENSP00000347978.4:p.Asp974Glu
ENST00000375954.1:c.621T>A (ERCC5) ENSP00000365121.1:p.Asp207Glu
ENST00000610537.4:c.2919T>A (ERCC5) ENSP00000478667.1:p.Asp973Glu
NM_000123.3:c.2922T>A , LRG_464t1:c.2922T>A (ERCC5) NP_000114.2:p.Asp974Glu
NM_001204425.1:c.4284T>A (BIVM-ERCC5) NP_001191354.1:p.Asp1428Glu
NM_000123.4:c.2922T>A (ERCC5) MANE Select NP_000114.3:p.Asp974Glu
NM_001204425.2:c.4284T>A (BIVM-ERCC5) NP_001191354.2:p.Asp1428Glu