Canonical Allele Identifier: CA413545459

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775096A>C (hg19) ; chrX:g.71555246A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555246A>C , CM000685.2:g.71555246A>C	GRCh38
NC_000023.10:g.70775096A>C , CM000685.1:g.70775096A>C	GRCh37
NC_000023.9:g.70691821A>C	NCBI36
NG_015875.1:g.27185A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.716A>C	ENSP00000514559.1:p.His239Pro
ENST00000699750.1:c.*644A>C	ENSP00000514560.1:n.*644A>C
ENST00000699751.1:n.1278+654A>C
ENST00000699779.1:c.*3653A>C	ENSP00000514585.1:n.*3653A>C
ENST00000699780.1:c.728+654A>C	ENSP00000514586.1:n.728+654A>C
ENST00000699781.1:c.*332+654A>C	ENSP00000514587.1:n.*332+654A>C
ENST00000699782.1:c.686A>C	ENSP00000514588.1:p.His229Pro
ENST00000699783.1:c.755A>C	ENSP00000514589.1:p.His252Pro
ENST00000699784.1:c.755A>C	ENSP00000514590.1:p.His252Pro
ENST00000699785.1:c.*790A>C	ENSP00000514591.1:n.*790A>C
ENST00000373719.8:c.785A>C MANE Select	ENSP00000362824.3:p.His262Pro
ENST00000373701.7:c.755A>C	ENSP00000362805.3:p.His252Pro
ENST00000373719.7:c.785A>C	ENSP00000362824.3:p.His262Pro
ENST00000459760.1:n.162A>C
ENST00000488174.5:n.4165+654A>C
NM_181672.2:c.785A>C	NP_858058.1:p.His262Pro
NM_181673.2:c.755A>C	NP_858059.1:p.His252Pro
XM_005262308.1:c.-220+654A>C	XP_005262365.1:n.-220+654A>C
XM_017029908.1:c.-220+654A>C	XP_016885397.1:n.-220+654A>C
XM_024452467.1:c.-220+654A>C	XP_024308235.1:n.-220+654A>C
NM_181672.3:c.785A>C MANE Select	NP_858058.1:p.His262Pro
NM_181673.3:c.755A>C	NP_858059.1:p.His252Pro