Canonical Allele Identifier: CA2115215408
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873441C= , CM000675.2:g.102873441C= GRCh38
NC_000013.10:g.103525791C= , CM000675.1:g.103525791C= GRCh37
NC_000013.9:g.102323792C= NCBI36
NG_007146.1:g.32618C= , LRG_464:g.32618C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4065+98C= (ERCC5)
ENST00000682869.1:n.3613+98C= (ERCC5)
ENST00000683246.1:n.4601+98C= (ERCC5)
ENST00000683642.1:n.3194+98C= (ERCC5)
ENST00000639132.1:c.3639+98C= (BIVM-ERCC5) ENSP00000492684.1:n.3639+98C=
ENST00000639435.1:c.4326+98C= (BIVM-ERCC5) ENSP00000491742.1:n.4326+98C=
ENST00000651002.1:c.*2725+98C= (ERCC5) ENSP00000498809.1:n.*2725+98C=
ENST00000651055.1:n.3091+98C= (ERCC5)
ENST00000651281.1:n.3332+98C= (ERCC5)
ENST00000651387.1:n.2448+98C= (ERCC5)
ENST00000651470.1:c.*136+98C= (ERCC5) ENSP00000498701.1:n.*136+98C=
ENST00000652225.2:c.2964+98C= (ERCC5) MANE Select ENSP00000498881.2:n.2964+98C=
ENST00000652613.1:c.2460+98C= (ERCC5) ENSP00000498357.1:n.2460+98C=
ENST00000355739.8:c.2964+98C= (ERCC5) ENSP00000347978.4:n.2964+98C=
ENST00000375954.1:c.663+98C= (ERCC5) ENSP00000365121.1:n.663+98C=
ENST00000610537.4:c.2961+98C= (ERCC5) ENSP00000478667.1:n.2961+98C=
NM_000123.3:c.2964+98C= , LRG_464t1:c.2964+98C= (ERCC5) NP_000114.2:n.2964+98C=
NM_001204425.1:c.4326+98C= (BIVM-ERCC5) NP_001191354.1:n.4326+98C=
NM_000123.4:c.2964+98C= (ERCC5) MANE Select NP_000114.3:n.2964+98C=
NM_001204425.2:c.4326+98C= (BIVM-ERCC5) NP_001191354.2:n.4326+98C=