Canonical Allele Identifier: CA388673508
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873290A>C , CM000675.2:g.102873290A>C GRCh38
NC_000013.10:g.103525640A>C , CM000675.1:g.103525640A>C GRCh37
NC_000013.9:g.102323641A>C NCBI36
NG_007146.1:g.32467A>C , LRG_464:g.32467A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4012A>C (ERCC5)
ENST00000682869.1:n.3560A>C (ERCC5)
ENST00000683246.1:n.4548A>C (ERCC5)
ENST00000683642.1:n.3141A>C (ERCC5)
ENST00000639132.1:c.3586A>C (BIVM-ERCC5) ENSP00000492684.1:p.Thr1196Pro
ENST00000639435.1:c.4273A>C (BIVM-ERCC5) ENSP00000491742.1:p.Thr1425Pro
ENST00000651002.1:c.*2672A>C (ERCC5) ENSP00000498809.1:n.*2672A>C
ENST00000651055.1:n.3038A>C (ERCC5)
ENST00000651281.1:n.3279A>C (ERCC5)
ENST00000651387.1:n.2395A>C (ERCC5)
ENST00000651470.1:c.*83A>C (ERCC5) ENSP00000498701.1:n.*83A>C
ENST00000652225.2:c.2911A>C (ERCC5) MANE Select ENSP00000498881.2:p.Thr971Pro
ENST00000652613.1:c.2407A>C (ERCC5) ENSP00000498357.1:p.Thr803Pro
ENST00000355739.8:c.2911A>C (ERCC5) ENSP00000347978.4:p.Thr971Pro
ENST00000375954.1:c.610A>C (ERCC5) ENSP00000365121.1:p.Thr204Pro
ENST00000610537.4:c.2908A>C (ERCC5) ENSP00000478667.1:p.Thr970Pro
NM_000123.3:c.2911A>C , LRG_464t1:c.2911A>C (ERCC5) NP_000114.2:p.Thr971Pro
NM_001204425.1:c.4273A>C (BIVM-ERCC5) NP_001191354.1:p.Thr1425Pro
NM_000123.4:c.2911A>C (ERCC5) MANE Select NP_000114.3:p.Thr971Pro
NM_001204425.2:c.4273A>C (BIVM-ERCC5) NP_001191354.2:p.Thr1425Pro