Canonical Allele Identifier: CA2436503725

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555236G= , CM000685.2:g.71555236G=	GRCh38
NC_000023.10:g.70775086G= , CM000685.1:g.70775086G=	GRCh37
NC_000023.9:g.70691811G=	NCBI36
NG_015875.1:g.27175G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.706G=	ENSP00000514559.1:p.Ala236=
ENST00000699750.1:c.*634G=	ENSP00000514560.1:n.*634G=
ENST00000699751.1:n.1278+644G=
ENST00000699779.1:c.*3643G=	ENSP00000514585.1:n.*3643G=
ENST00000699780.1:c.728+644G=	ENSP00000514586.1:n.728+644G=
ENST00000699781.1:c.*332+644G=	ENSP00000514587.1:n.*332+644G=
ENST00000699782.1:c.676G=	ENSP00000514588.1:p.Ala226=
ENST00000699783.1:c.745G=	ENSP00000514589.1:p.Ala249=
ENST00000699784.1:c.745G=	ENSP00000514590.1:p.Ala249=
ENST00000699785.1:c.*780G=	ENSP00000514591.1:n.*780G=
ENST00000373719.8:c.775G= MANE Select	ENSP00000362824.3:p.Ala259=
ENST00000373701.7:c.745G=	ENSP00000362805.3:p.Ala249=
ENST00000373719.7:c.775G=	ENSP00000362824.3:p.Ala259=
ENST00000459760.1:n.152G=
ENST00000488174.5:n.4165+644G=
NM_181672.2:c.775G=	NP_858058.1:p.Ala259=
NM_181673.2:c.745G=	NP_858059.1:p.Ala249=
XM_005262308.1:c.-220+644G=	XP_005262365.1:n.-220+644G=
XM_017029908.1:c.-220+644G=	XP_016885397.1:n.-220+644G=
XM_024452467.1:c.-220+644G=	XP_024308235.1:n.-220+644G=
NM_181672.3:c.775G= MANE Select	NP_858058.1:p.Ala259=
NM_181673.3:c.745G=	NP_858059.1:p.Ala249=