Canonical Allele Identifier: CA1479860704

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127283G= , CM000666.2:g.99127283G=	GRCh38
NC_000004.11:g.100048434G= , CM000666.1:g.100048434G=	GRCh37
NC_000004.10:g.100267457G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.905C= MANE Select	ENSP00000265512.7:p.Ala302=
ENST00000265512.11:c.905C=	ENSP00000265512.7:p.Ala302=
ENST00000505590.5:c.962C=	ENSP00000425416.1:p.Ala321=
ENST00000506705.5:c.*879C=	ENSP00000426667.1:n.*879C=
ENST00000508393.5:c.962C=	ENSP00000424630.1:p.Ala321=
ENST00000509471.5:c.334-551C=	ENSP00000424583.1:n.334-551C=
ENST00000629236.2:c.905C=	ENSP00000486450.1:p.Ala302=
NM_000670.3:c.905C=	NP_000661.2:p.Ala302=
NM_000670.4:c.905C=	NP_000661.2:p.Ala302=
NM_001306171.1:c.962C=	NP_001293100.1:p.Ala321=
NM_001306172.1:c.962C=	NP_001293101.1:p.Ala321=
NR_037884.1:n.429-6272G=
XR_938685.1:n.1133C=
XR_938686.1:n.1124C=
XR_938687.1:n.997C=
NM_000670.5:c.905C= MANE Select	NP_000661.2:p.Ala302=
NM_001306171.2:c.962C=	NP_001293100.1:p.Ala321=
NM_001306172.2:c.962C=	NP_001293101.1:p.Ala321=