Canonical Allele Identifier: CA388675121
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875662G>C , CM000675.2:g.102875662G>C GRCh38
NC_000013.10:g.103528012G>C , CM000675.1:g.103528012G>C GRCh37
NC_000013.9:g.102326013G>C NCBI36
NG_007146.1:g.34839G>C , LRG_464:g.34839G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4421G>C (ERCC5)
ENST00000682869.1:n.3969G>C (ERCC5)
ENST00000683246.1:n.4957G>C (ERCC5)
ENST00000683642.1:n.3550G>C (ERCC5)
ENST00000639132.1:c.3995G>C (BIVM-ERCC5) ENSP00000492684.1:p.Ser1332Thr
ENST00000639435.1:c.4682G>C (BIVM-ERCC5) ENSP00000491742.1:p.Ser1561Thr
ENST00000651002.1:c.*3081G>C (ERCC5) ENSP00000498809.1:n.*3081G>C
ENST00000651055.1:n.3447G>C (ERCC5)
ENST00000651281.1:n.3688G>C (ERCC5)
ENST00000651387.1:n.2804G>C (ERCC5)
ENST00000651470.1:c.*492G>C (ERCC5) ENSP00000498701.1:n.*492G>C
ENST00000652225.2:c.3320G>C (ERCC5) MANE Select ENSP00000498881.2:p.Ser1107Thr
ENST00000652613.1:c.2816G>C (ERCC5) ENSP00000498357.1:p.Ser939Thr
ENST00000355739.8:c.3320G>C (ERCC5) ENSP00000347978.4:p.Ser1107Thr
ENST00000375954.1:c.1019G>C (ERCC5) ENSP00000365121.1:p.Ser340Thr
ENST00000472247.1:n.480G>C (ERCC5)
ENST00000610537.4:c.3317G>C (ERCC5) ENSP00000478667.1:p.Ser1106Thr
NM_000123.3:c.3320G>C , LRG_464t1:c.3320G>C (ERCC5) NP_000114.2:p.Ser1107Thr
NM_001204425.1:c.4682G>C (BIVM-ERCC5) NP_001191354.1:p.Ser1561Thr
NM_000123.4:c.3320G>C (ERCC5) MANE Select NP_000114.3:p.Ser1107Thr
NM_001204425.2:c.4682G>C (BIVM-ERCC5) NP_001191354.2:p.Ser1561Thr