Canonical Allele Identifier: CA388675066
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875637G>T , CM000675.2:g.102875637G>T GRCh38
NC_000013.10:g.103527987G>T , CM000675.1:g.103527987G>T GRCh37
NC_000013.9:g.102325988G>T NCBI36
NG_007146.1:g.34814G>T , LRG_464:g.34814G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4396G>T (ERCC5)
ENST00000682869.1:n.3944G>T (ERCC5)
ENST00000683246.1:n.4932G>T (ERCC5)
ENST00000683642.1:n.3525G>T (ERCC5)
ENST00000639132.1:c.3970G>T (BIVM-ERCC5) ENSP00000492684.1:p.Gly1324Ter
ENST00000639435.1:c.4657G>T (BIVM-ERCC5) ENSP00000491742.1:p.Gly1553Ter
ENST00000651002.1:c.*3056G>T (ERCC5) ENSP00000498809.1:n.*3056G>T
ENST00000651055.1:n.3422G>T (ERCC5)
ENST00000651281.1:n.3663G>T (ERCC5)
ENST00000651387.1:n.2779G>T (ERCC5)
ENST00000651470.1:c.*467G>T (ERCC5) ENSP00000498701.1:n.*467G>T
ENST00000652225.2:c.3295G>T (ERCC5) MANE Select ENSP00000498881.2:p.Gly1099Ter
ENST00000652613.1:c.2791G>T (ERCC5) ENSP00000498357.1:p.Gly931Ter
ENST00000355739.8:c.3295G>T (ERCC5) ENSP00000347978.4:p.Gly1099Ter
ENST00000375954.1:c.994G>T (ERCC5) ENSP00000365121.1:p.Gly332Ter
ENST00000472247.1:n.455G>T (ERCC5)
ENST00000610537.4:c.3292G>T (ERCC5) ENSP00000478667.1:p.Gly1098Ter
NM_000123.3:c.3295G>T , LRG_464t1:c.3295G>T (ERCC5) NP_000114.2:p.Gly1099Ter
NM_001204425.1:c.4657G>T (BIVM-ERCC5) NP_001191354.1:p.Gly1553Ter
NM_000123.4:c.3295G>T (ERCC5) MANE Select NP_000114.3:p.Gly1099Ter
NM_001204425.2:c.4657G>T (BIVM-ERCC5) NP_001191354.2:p.Gly1553Ter