Canonical Allele Identifier: CA388673510
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873291C>A , CM000675.2:g.102873291C>A GRCh38
NC_000013.10:g.103525641C>A , CM000675.1:g.103525641C>A GRCh37
NC_000013.9:g.102323642C>A NCBI36
NG_007146.1:g.32468C>A , LRG_464:g.32468C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4013C>A (ERCC5)
ENST00000682869.1:n.3561C>A (ERCC5)
ENST00000683246.1:n.4549C>A (ERCC5)
ENST00000683642.1:n.3142C>A (ERCC5)
ENST00000639132.1:c.3587C>A (BIVM-ERCC5) ENSP00000492684.1:p.Thr1196Lys
ENST00000639435.1:c.4274C>A (BIVM-ERCC5) ENSP00000491742.1:p.Thr1425Lys
ENST00000651002.1:c.*2673C>A (ERCC5) ENSP00000498809.1:n.*2673C>A
ENST00000651055.1:n.3039C>A (ERCC5)
ENST00000651281.1:n.3280C>A (ERCC5)
ENST00000651387.1:n.2396C>A (ERCC5)
ENST00000651470.1:c.*84C>A (ERCC5) ENSP00000498701.1:n.*84C>A
ENST00000652225.2:c.2912C>A (ERCC5) MANE Select ENSP00000498881.2:p.Thr971Lys
ENST00000652613.1:c.2408C>A (ERCC5) ENSP00000498357.1:p.Thr803Lys
ENST00000355739.8:c.2912C>A (ERCC5) ENSP00000347978.4:p.Thr971Lys
ENST00000375954.1:c.611C>A (ERCC5) ENSP00000365121.1:p.Thr204Lys
ENST00000610537.4:c.2909C>A (ERCC5) ENSP00000478667.1:p.Thr970Lys
NM_000123.3:c.2912C>A , LRG_464t1:c.2912C>A (ERCC5) NP_000114.2:p.Thr971Lys
NM_001204425.1:c.4274C>A (BIVM-ERCC5) NP_001191354.1:p.Thr1425Lys
NM_000123.4:c.2912C>A (ERCC5) MANE Select NP_000114.3:p.Thr971Lys
NM_001204425.2:c.4274C>A (BIVM-ERCC5) NP_001191354.2:p.Thr1425Lys