Canonical Allele Identifier: CA1479860731

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127338C= , CM000666.2:g.99127338C=	GRCh38
NC_000004.11:g.100048489C= , CM000666.1:g.100048489C=	GRCh37
NC_000004.10:g.100267512C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.850G= MANE Select	ENSP00000265512.7:p.Ala284=
ENST00000265512.11:c.850G=	ENSP00000265512.7:p.Ala284=
ENST00000505590.5:c.907G=	ENSP00000425416.1:p.Ala303=
ENST00000506705.5:c.*824G=	ENSP00000426667.1:n.*824G=
ENST00000508393.5:c.907G=	ENSP00000424630.1:p.Ala303=
ENST00000509471.5:c.334-606G=	ENSP00000424583.1:n.334-606G=
ENST00000629236.2:c.850G=	ENSP00000486450.1:p.Ala284=
NM_000670.3:c.850G=	NP_000661.2:p.Ala284=
NM_000670.4:c.850G=	NP_000661.2:p.Ala284=
NM_001306171.1:c.907G=	NP_001293100.1:p.Ala303=
NM_001306172.1:c.907G=	NP_001293101.1:p.Ala303=
NR_037884.1:n.429-6217C=
XR_938685.1:n.1078G=
XR_938686.1:n.1069G=
XR_938687.1:n.942G=
NM_000670.5:c.850G= MANE Select	NP_000661.2:p.Ala284=
NM_001306171.2:c.907G=	NP_001293100.1:p.Ala303=
NM_001306172.2:c.907G=	NP_001293101.1:p.Ala303=