Canonical Allele Identifier: CA1479840646

Gene: ADH5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99077829G= , CM000666.2:g.99077829G=	GRCh38
NC_000004.11:g.99998980G= , CM000666.1:g.99998980G=	GRCh37
NC_000004.10:g.100218003G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296412.14:c.345-906C= MANE Select	ENSP00000296412.8:n.345-906C=
ENST00000296412.13:c.345-906C=	ENSP00000296412.8:n.345-906C=
ENST00000296412.12:c.345-906C=	ENSP00000296412.8:n.345-906C=
ENST00000502590.5:c.*25-906C=	ENSP00000422119.1:n.*25-906C=
ENST00000503130.5:c.306-906C=	ENSP00000427049.1:n.306-906C=
ENST00000505652.1:c.*169-906C=	ENSP00000421556.1:n.*169-906C=
ENST00000508511.5:n.362-906C=
ENST00000512604.1:n.205-906C=
ENST00000512621.5:n.333-906C=
ENST00000512659.5:c.*32-906C=	ENSP00000424650.1:n.*32-906C=
ENST00000512991.5:n.543-906C=
ENST00000626055.2:c.*32-906C=	ENSP00000487496.1:n.*32-906C=
NM_000671.4:c.345-906C= MANE Select	NP_000662.3:n.345-906C=