Canonical Allele Identifier: CA2436503805

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555606C= , CM000685.2:g.71555606C=	GRCh38
NC_000023.10:g.70775456C= , CM000685.1:g.70775456C=	GRCh37
NC_000023.9:g.70692181C=	NCBI36
NG_015875.1:g.27545C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.855+221C=	ENSP00000514559.1:n.855+221C=
ENST00000699750.1:c.*783+221C=	ENSP00000514560.1:n.*783+221C=
ENST00000699751.1:n.1278+1014C=
ENST00000699779.1:c.*3792+221C=	ENSP00000514585.1:n.*3792+221C=
ENST00000699780.1:c.729-348C=	ENSP00000514586.1:n.729-348C=
ENST00000699781.1:c.*333-348C=	ENSP00000514587.1:n.*333-348C=
ENST00000699782.1:c.825+221C=	ENSP00000514588.1:n.825+221C=
ENST00000699783.1:c.894+221C=	ENSP00000514589.1:n.894+221C=
ENST00000699784.1:c.894+221C=	ENSP00000514590.1:n.894+221C=
ENST00000699785.1:c.*929+221C=	ENSP00000514591.1:n.*929+221C=
ENST00000373719.8:c.924+221C= MANE Select	ENSP00000362824.3:n.924+221C=
ENST00000373701.7:c.894+221C=	ENSP00000362805.3:n.894+221C=
ENST00000373719.7:c.924+221C=	ENSP00000362824.3:n.924+221C=
ENST00000459760.1:n.301+221C=
ENST00000488174.5:n.4166-348C=
NM_181672.2:c.924+221C=	NP_858058.1:n.924+221C=
NM_181673.2:c.894+221C=	NP_858059.1:n.894+221C=
XM_005262308.1:c.-219-348C=	XP_005262365.1:n.-219-348C=
XM_017029908.1:c.-219-348C=	XP_016885397.1:n.-219-348C=
XM_024452467.1:c.-219-348C=	XP_024308235.1:n.-219-348C=
NM_181672.3:c.924+221C= MANE Select	NP_858058.1:n.924+221C=
NM_181673.3:c.894+221C=	NP_858059.1:n.894+221C=