Canonical Allele Identifier: CA2115211007

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102862879T= , CM000675.2:g.102862879T=	GRCh38
NC_000013.10:g.103515229T= , CM000675.1:g.103515229T=	GRCh37
NC_000013.9:g.102313230T=	NCBI36
NG_007146.1:g.22056T= , LRG_464:g.22056T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.1971T= (ERCC5)
ENST00000682869.1:n.2379T= (ERCC5)
ENST00000683246.1:n.2507T= (ERCC5)
ENST00000639132.1:c.2405T= (BIVM-ERCC5)	ENSP00000492684.1:p.Val802=
ENST00000639435.1:c.3092T= (BIVM-ERCC5)	ENSP00000491742.1:p.Val1031=
ENST00000651002.1:c.*1491T= (ERCC5)	ENSP00000498809.1:n.*1491T=
ENST00000651055.1:n.1859T= (ERCC5)
ENST00000651281.1:n.2098T= (ERCC5)
ENST00000651387.1:n.1214T= (ERCC5)
ENST00000651470.1:c.1730T= (ERCC5)	ENSP00000498701.1:p.Val577=
ENST00000652225.2:c.1730T= (ERCC5) MANE Select	ENSP00000498881.2:p.Val577=
ENST00000652613.1:c.1226T= (ERCC5)	ENSP00000498357.1:p.Val409=
ENST00000355739.8:c.1730T= (ERCC5)	ENSP00000347978.4:p.Val577=
ENST00000602836.1:c.3006T= (BIVM-ERCC5)
ENST00000610537.4:c.1730T= (ERCC5)	ENSP00000478667.1:p.Val577=
NM_000123.3:c.1730T= , LRG_464t1:c.1730T= (ERCC5)	NP_000114.2:p.Val577=
NM_001204425.1:c.3092T= (BIVM-ERCC5)	NP_001191354.1:p.Val1031=
NM_000123.4:c.1730T= (ERCC5) MANE Select	NP_000114.3:p.Val577=
NM_001204425.2:c.3092T= (BIVM-ERCC5)	NP_001191354.2:p.Val1031=