Canonical Allele Identifier: CA2436503722

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555223G= , CM000685.2:g.71555223G=	GRCh38
NC_000023.10:g.70775073G= , CM000685.1:g.70775073G=	GRCh37
NC_000023.9:g.70691798G=	NCBI36
NG_015875.1:g.27162G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.693G=	ENSP00000514559.1:p.Leu231=
ENST00000699750.1:c.*621G=	ENSP00000514560.1:n.*621G=
ENST00000699751.1:n.1278+631G=
ENST00000699779.1:c.*3630G=	ENSP00000514585.1:n.*3630G=
ENST00000699780.1:c.728+631G=	ENSP00000514586.1:n.728+631G=
ENST00000699781.1:c.*332+631G=	ENSP00000514587.1:n.*332+631G=
ENST00000699782.1:c.663G=	ENSP00000514588.1:p.Leu221=
ENST00000699783.1:c.732G=	ENSP00000514589.1:p.Leu244=
ENST00000699784.1:c.732G=	ENSP00000514590.1:p.Leu244=
ENST00000699785.1:c.*767G=	ENSP00000514591.1:n.*767G=
ENST00000373719.8:c.762G= MANE Select	ENSP00000362824.3:p.Leu254=
ENST00000373701.7:c.732G=	ENSP00000362805.3:p.Leu244=
ENST00000373719.7:c.762G=	ENSP00000362824.3:p.Leu254=
ENST00000459760.1:n.139G=
ENST00000488174.5:n.4165+631G=
NM_181672.2:c.762G=	NP_858058.1:p.Leu254=
NM_181673.2:c.732G=	NP_858059.1:p.Leu244=
XM_005262308.1:c.-220+631G=	XP_005262365.1:n.-220+631G=
XM_017029908.1:c.-220+631G=	XP_016885397.1:n.-220+631G=
XM_024452467.1:c.-220+631G=	XP_024308235.1:n.-220+631G=
NM_181672.3:c.762G= MANE Select	NP_858058.1:p.Leu254=
NM_181673.3:c.732G=	NP_858059.1:p.Leu244=