Canonical Allele Identifier: CA388674994
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875603T>A , CM000675.2:g.102875603T>A GRCh38
NC_000013.10:g.103527953T>A , CM000675.1:g.103527953T>A GRCh37
NC_000013.9:g.102325954T>A NCBI36
NG_007146.1:g.34780T>A , LRG_464:g.34780T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4362T>A (ERCC5)
ENST00000682869.1:n.3910T>A (ERCC5)
ENST00000683246.1:n.4898T>A (ERCC5)
ENST00000683642.1:n.3491T>A (ERCC5)
ENST00000639132.1:c.3936T>A (BIVM-ERCC5) ENSP00000492684.1:p.Phe1312Leu
ENST00000639435.1:c.4623T>A (BIVM-ERCC5) ENSP00000491742.1:p.Phe1541Leu
ENST00000651002.1:c.*3022T>A (ERCC5) ENSP00000498809.1:n.*3022T>A
ENST00000651055.1:n.3388T>A (ERCC5)
ENST00000651281.1:n.3629T>A (ERCC5)
ENST00000651387.1:n.2745T>A (ERCC5)
ENST00000651470.1:c.*433T>A (ERCC5) ENSP00000498701.1:n.*433T>A
ENST00000652225.2:c.3261T>A (ERCC5) MANE Select ENSP00000498881.2:p.Phe1087Leu
ENST00000652613.1:c.2757T>A (ERCC5) ENSP00000498357.1:p.Phe919Leu
ENST00000355739.8:c.3261T>A (ERCC5) ENSP00000347978.4:p.Phe1087Leu
ENST00000375954.1:c.960T>A (ERCC5) ENSP00000365121.1:p.Phe320Leu
ENST00000472247.1:n.421T>A (ERCC5)
ENST00000610537.4:c.3258T>A (ERCC5) ENSP00000478667.1:p.Phe1086Leu
NM_000123.3:c.3261T>A , LRG_464t1:c.3261T>A (ERCC5) NP_000114.2:p.Phe1087Leu
NM_001204425.1:c.4623T>A (BIVM-ERCC5) NP_001191354.1:p.Phe1541Leu
NM_000123.4:c.3261T>A (ERCC5) MANE Select NP_000114.3:p.Phe1087Leu
NM_001204425.2:c.4623T>A (BIVM-ERCC5) NP_001191354.2:p.Phe1541Leu