Canonical Allele Identifier: CA1479860719

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127311C= , CM000666.2:g.99127311C=	GRCh38
NC_000004.11:g.100048462C= , CM000666.1:g.100048462C=	GRCh37
NC_000004.10:g.100267485C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.877G= MANE Select	ENSP00000265512.7:p.Gly293=
ENST00000265512.11:c.877G=	ENSP00000265512.7:p.Gly293=
ENST00000505590.5:c.934G=	ENSP00000425416.1:p.Gly312=
ENST00000506705.5:c.*851G=	ENSP00000426667.1:n.*851G=
ENST00000508393.5:c.934G=	ENSP00000424630.1:p.Gly312=
ENST00000509471.5:c.334-579G=	ENSP00000424583.1:n.334-579G=
ENST00000629236.2:c.877G=	ENSP00000486450.1:p.Gly293=
NM_000670.3:c.877G=	NP_000661.2:p.Gly293=
NM_000670.4:c.877G=	NP_000661.2:p.Gly293=
NM_001306171.1:c.934G=	NP_001293100.1:p.Gly312=
NM_001306172.1:c.934G=	NP_001293101.1:p.Gly312=
NR_037884.1:n.429-6244C=
XR_938685.1:n.1105G=
XR_938686.1:n.1096G=
XR_938687.1:n.969G=
NM_000670.5:c.877G= MANE Select	NP_000661.2:p.Gly293=
NM_001306171.2:c.934G=	NP_001293100.1:p.Gly312=
NM_001306172.2:c.934G=	NP_001293101.1:p.Gly312=