Canonical Allele Identifier: CA388675063
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875636T>G , CM000675.2:g.102875636T>G GRCh38
NC_000013.10:g.103527986T>G , CM000675.1:g.103527986T>G GRCh37
NC_000013.9:g.102325987T>G NCBI36
NG_007146.1:g.34813T>G , LRG_464:g.34813T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4395T>G (ERCC5)
ENST00000682869.1:n.3943T>G (ERCC5)
ENST00000683246.1:n.4931T>G (ERCC5)
ENST00000683642.1:n.3524T>G (ERCC5)
ENST00000639132.1:c.3969T>G (BIVM-ERCC5) ENSP00000492684.1:p.Asp1323Glu
ENST00000639435.1:c.4656T>G (BIVM-ERCC5) ENSP00000491742.1:p.Asp1552Glu
ENST00000651002.1:c.*3055T>G (ERCC5) ENSP00000498809.1:n.*3055T>G
ENST00000651055.1:n.3421T>G (ERCC5)
ENST00000651281.1:n.3662T>G (ERCC5)
ENST00000651387.1:n.2778T>G (ERCC5)
ENST00000651470.1:c.*466T>G (ERCC5) ENSP00000498701.1:n.*466T>G
ENST00000652225.2:c.3294T>G (ERCC5) MANE Select ENSP00000498881.2:p.Asp1098Glu
ENST00000652613.1:c.2790T>G (ERCC5) ENSP00000498357.1:p.Asp930Glu
ENST00000355739.8:c.3294T>G (ERCC5) ENSP00000347978.4:p.Asp1098Glu
ENST00000375954.1:c.993T>G (ERCC5) ENSP00000365121.1:p.Asp331Glu
ENST00000472247.1:n.454T>G (ERCC5)
ENST00000610537.4:c.3291T>G (ERCC5) ENSP00000478667.1:p.Asp1097Glu
NM_000123.3:c.3294T>G , LRG_464t1:c.3294T>G (ERCC5) NP_000114.2:p.Asp1098Glu
NM_001204425.1:c.4656T>G (BIVM-ERCC5) NP_001191354.1:p.Asp1552Glu
NM_000123.4:c.3294T>G (ERCC5) MANE Select NP_000114.3:p.Asp1098Glu
NM_001204425.2:c.4656T>G (BIVM-ERCC5) NP_001191354.2:p.Asp1552Glu