Canonical Allele Identifier: CA2436503738

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555331A= , CM000685.2:g.71555331A=	GRCh38
NC_000023.10:g.70775181A= , CM000685.1:g.70775181A=	GRCh37
NC_000023.9:g.70691906A=	NCBI36
NG_015875.1:g.27270A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.801A=	ENSP00000514559.1:p.Pro267=
ENST00000699750.1:c.*729A=	ENSP00000514560.1:n.*729A=
ENST00000699751.1:n.1278+739A=
ENST00000699779.1:c.*3738A=	ENSP00000514585.1:n.*3738A=
ENST00000699780.1:c.729-623A=	ENSP00000514586.1:n.729-623A=
ENST00000699781.1:c.*333-623A=	ENSP00000514587.1:n.*333-623A=
ENST00000699782.1:c.771A=	ENSP00000514588.1:p.Pro257=
ENST00000699783.1:c.840A=	ENSP00000514589.1:p.Pro280=
ENST00000699784.1:c.840A=	ENSP00000514590.1:p.Pro280=
ENST00000699785.1:c.*875A=	ENSP00000514591.1:n.*875A=
ENST00000373719.8:c.870A= MANE Select	ENSP00000362824.3:p.Pro290=
ENST00000373701.7:c.840A=	ENSP00000362805.3:p.Pro280=
ENST00000373719.7:c.870A=	ENSP00000362824.3:p.Pro290=
ENST00000459760.1:n.247A=
ENST00000488174.5:n.4166-623A=
NM_181672.2:c.870A=	NP_858058.1:p.Pro290=
NM_181673.2:c.840A=	NP_858059.1:p.Pro280=
XM_005262308.1:c.-219-623A=	XP_005262365.1:n.-219-623A=
XM_017029908.1:c.-219-623A=	XP_016885397.1:n.-219-623A=
XM_024452467.1:c.-219-623A=	XP_024308235.1:n.-219-623A=
NM_181672.3:c.870A= MANE Select	NP_858058.1:p.Pro290=
NM_181673.3:c.840A=	NP_858059.1:p.Pro280=