Canonical Allele Identifier: CA2436503745

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555376G= , CM000685.2:g.71555376G=	GRCh38
NC_000023.10:g.70775226G= , CM000685.1:g.70775226G=	GRCh37
NC_000023.9:g.70691951G=	NCBI36
NG_015875.1:g.27315G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.846G=	ENSP00000514559.1:p.Glu282=
ENST00000699750.1:c.*774G=	ENSP00000514560.1:n.*774G=
ENST00000699751.1:n.1278+784G=
ENST00000699779.1:c.*3783G=	ENSP00000514585.1:n.*3783G=
ENST00000699780.1:c.729-578G=	ENSP00000514586.1:n.729-578G=
ENST00000699781.1:c.*333-578G=	ENSP00000514587.1:n.*333-578G=
ENST00000699782.1:c.816G=	ENSP00000514588.1:p.Glu272=
ENST00000699783.1:c.885G=	ENSP00000514589.1:p.Glu295=
ENST00000699784.1:c.885G=	ENSP00000514590.1:p.Glu295=
ENST00000699785.1:c.*920G=	ENSP00000514591.1:n.*920G=
ENST00000373719.8:c.915G= MANE Select	ENSP00000362824.3:p.Glu305=
ENST00000373701.7:c.885G=	ENSP00000362805.3:p.Glu295=
ENST00000373719.7:c.915G=	ENSP00000362824.3:p.Glu305=
ENST00000459760.1:n.292G=
ENST00000488174.5:n.4166-578G=
NM_181672.2:c.915G=	NP_858058.1:p.Glu305=
NM_181673.2:c.885G=	NP_858059.1:p.Glu295=
XM_005262308.1:c.-219-578G=	XP_005262365.1:n.-219-578G=
XM_017029908.1:c.-219-578G=	XP_016885397.1:n.-219-578G=
XM_024452467.1:c.-219-578G=	XP_024308235.1:n.-219-578G=
NM_181672.3:c.915G= MANE Select	NP_858058.1:p.Glu305=
NM_181673.3:c.885G=	NP_858059.1:p.Glu295=