Canonical Allele Identifier: CA1479860695

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127264A= , CM000666.2:g.99127264A=	GRCh38
NC_000004.11:g.100048415A= , CM000666.1:g.100048415A=	GRCh37
NC_000004.10:g.100267438A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.924T= MANE Select	ENSP00000265512.7:p.Thr308=
ENST00000265512.11:c.924T=	ENSP00000265512.7:p.Thr308=
ENST00000505590.5:c.981T=	ENSP00000425416.1:p.Thr327=
ENST00000506705.5:c.*898T=	ENSP00000426667.1:n.*898T=
ENST00000508393.5:c.981T=	ENSP00000424630.1:p.Thr327=
ENST00000509471.5:c.334-532T=	ENSP00000424583.1:n.334-532T=
ENST00000629236.2:c.924T=	ENSP00000486450.1:p.Thr308=
NM_000670.3:c.924T=	NP_000661.2:p.Thr308=
NM_000670.4:c.924T=	NP_000661.2:p.Thr308=
NM_001306171.1:c.981T=	NP_001293100.1:p.Thr327=
NM_001306172.1:c.981T=	NP_001293101.1:p.Thr327=
NR_037884.1:n.429-6291A=
XR_938685.1:n.1152T=
XR_938686.1:n.1143T=
XR_938687.1:n.1016T=
NM_000670.5:c.924T= MANE Select	NP_000661.2:p.Thr308=
NM_001306171.2:c.981T=	NP_001293100.1:p.Thr327=
NM_001306172.2:c.981T=	NP_001293101.1:p.Thr327=