Canonical Allele Identifier: CA2018008113
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875652G= , CM000675.2:g.102875652G= GRCh38
NC_000013.10:g.103528002G= , CM000675.1:g.103528002G= GRCh37
NC_000013.9:g.102326003G= NCBI36
NG_007146.1:g.34829G= , LRG_464:g.34829G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4411G= (ERCC5)
ENST00000682869.1:n.3959G= (ERCC5)
ENST00000683246.1:n.4947G= (ERCC5)
ENST00000683642.1:n.3540G= (ERCC5)
ENST00000639132.1:c.3985G= (BIVM-ERCC5) ENSP00000492684.1:p.Asp1329=
ENST00000639435.1:c.4672G= (BIVM-ERCC5) ENSP00000491742.1:p.Asp1558=
ENST00000651002.1:c.*3071G= (ERCC5) ENSP00000498809.1:n.*3071G=
ENST00000651055.1:n.3437G= (ERCC5)
ENST00000651281.1:n.3678G= (ERCC5)
ENST00000651387.1:n.2794G= (ERCC5)
ENST00000651470.1:c.*482G= (ERCC5) ENSP00000498701.1:n.*482G=
ENST00000652225.2:c.3310G= (ERCC5) MANE Select ENSP00000498881.2:p.Asp1104=
ENST00000652613.1:c.2806G= (ERCC5) ENSP00000498357.1:p.Asp936=
ENST00000355739.8:c.3310G= (ERCC5) ENSP00000347978.4:p.Asp1104=
ENST00000375954.1:c.1009G= (ERCC5) ENSP00000365121.1:p.Asp337=
ENST00000472247.1:n.470G= (ERCC5)
ENST00000610537.4:c.3307G= (ERCC5) ENSP00000478667.1:p.Asp1103=
NM_000123.3:c.3310G= , LRG_464t1:c.3310G= (ERCC5) NP_000114.2:p.Asp1104=
NM_001204425.1:c.4672G= (BIVM-ERCC5) NP_001191354.1:p.Asp1558=
NM_000123.4:c.3310G= (ERCC5) MANE Select NP_000114.3:p.Asp1104=
NM_001204425.2:c.4672G= (BIVM-ERCC5) NP_001191354.2:p.Asp1558=