Canonical Allele Identifier: CA1479860402

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126600C= , CM000666.2:g.99126600C=	GRCh38
NC_000004.11:g.100047751C= , CM000666.1:g.100047751C=	GRCh37
NC_000004.10:g.100266774C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1112G= MANE Select	ENSP00000265512.7:p.Gly371=
ENST00000265512.11:c.1112G=	ENSP00000265512.7:p.Gly371=
ENST00000505590.5:c.1169G=	ENSP00000425416.1:p.Gly390=
ENST00000506705.5:c.*1086G=	ENSP00000426667.1:n.*1086G=
ENST00000508393.5:c.1169G=	ENSP00000424630.1:p.Gly390=
ENST00000509471.5:c.466G=	ENSP00000424583.1:n.466G=
ENST00000629236.2:c.1112G=	ENSP00000486450.1:p.Gly371=
NM_000670.3:c.1112G=	NP_000661.2:p.Gly371=
NM_000670.4:c.1112G=	NP_000661.2:p.Gly371=
NM_001306171.1:c.1169G=	NP_001293100.1:p.Gly390=
NM_001306172.1:c.1169G=	NP_001293101.1:p.Gly390=
NR_037884.1:n.429-6955C=
XR_938685.1:n.1340G=
XR_938686.1:n.1331G=
XR_938687.1:n.1204G=
NM_000670.5:c.1112G= MANE Select	NP_000661.2:p.Gly371=
NM_001306171.2:c.1169G=	NP_001293100.1:p.Gly390=
NM_001306172.2:c.1169G=	NP_001293101.1:p.Gly390=