Canonical Allele Identifier: CA2436503731

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555312G= , CM000685.2:g.71555312G=	GRCh38
NC_000023.10:g.70775162G= , CM000685.1:g.70775162G=	GRCh37
NC_000023.9:g.70691887G=	NCBI36
NG_015875.1:g.27251G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.782G=	ENSP00000514559.1:p.Arg261=
ENST00000699750.1:c.*710G=	ENSP00000514560.1:n.*710G=
ENST00000699751.1:n.1278+720G=
ENST00000699779.1:c.*3719G=	ENSP00000514585.1:n.*3719G=
ENST00000699780.1:c.729-642G=	ENSP00000514586.1:n.729-642G=
ENST00000699781.1:c.*333-642G=	ENSP00000514587.1:n.*333-642G=
ENST00000699782.1:c.752G=	ENSP00000514588.1:p.Arg251=
ENST00000699783.1:c.821G=	ENSP00000514589.1:p.Arg274=
ENST00000699784.1:c.821G=	ENSP00000514590.1:p.Arg274=
ENST00000699785.1:c.*856G=	ENSP00000514591.1:n.*856G=
ENST00000373719.8:c.851G= MANE Select	ENSP00000362824.3:p.Arg284=
ENST00000373701.7:c.821G=	ENSP00000362805.3:p.Arg274=
ENST00000373719.7:c.851G=	ENSP00000362824.3:p.Arg284=
ENST00000459760.1:n.228G=
ENST00000488174.5:n.4166-642G=
NM_181672.2:c.851G=	NP_858058.1:p.Arg284=
NM_181673.2:c.821G=	NP_858059.1:p.Arg274=
XM_005262308.1:c.-219-642G=	XP_005262365.1:n.-219-642G=
XM_017029908.1:c.-219-642G=	XP_016885397.1:n.-219-642G=
XM_024452467.1:c.-219-642G=	XP_024308235.1:n.-219-642G=
NM_181672.3:c.851G= MANE Select	NP_858058.1:p.Arg284=
NM_181673.3:c.821G=	NP_858059.1:p.Arg274=