Canonical Allele Identifier: CA877838222

Gene: OGT

Linked Data

• dbSNP Id: rs1307980051
• MyVariant Identifiers: chrX:g.70774982_70774983insTG (hg19) ; chrX:g.71555132_71555133insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555133_71555134insGT , CM000685.2:g.71555133_71555134insGT	GRCh38
NC_000023.10:g.70774983_70774984insGT , CM000685.1:g.70774983_70774984insGT	GRCh37
NC_000023.9:g.70691708_70691709insGT	NCBI36
NG_015875.1:g.27072_27073insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-57_660-56insGT	ENSP00000514559.1:n.660-57_660-56insGT
ENST00000699750.1:c.*588-57_*588-56insGT	ENSP00000514560.1:n.*588-57_*588-56insGT
ENST00000699751.1:n.1278+541_1278+542insGT
ENST00000699779.1:c.*3597-57_*3597-56insGT	ENSP00000514585.1:n.*3597-57_*3597-56insGT
ENST00000699780.1:c.728+541_728+542insGT	ENSP00000514586.1:n.728+541_728+542insGT
ENST00000699781.1:c.*332+541_*332+542insGT	ENSP00000514587.1:n.*332+541_*332+542insGT
ENST00000699782.1:c.630-57_630-56insGT	ENSP00000514588.1:n.630-57_630-56insGT
ENST00000699783.1:c.699-57_699-56insGT	ENSP00000514589.1:n.699-57_699-56insGT
ENST00000699784.1:c.699-57_699-56insGT	ENSP00000514590.1:n.699-57_699-56insGT
ENST00000699785.1:c.*734-57_*734-56insGT	ENSP00000514591.1:n.*734-57_*734-56insGT
ENST00000373719.8:c.729-57_729-56insGT MANE Select	ENSP00000362824.3:n.729-57_729-56insGT
ENST00000373701.7:c.699-57_699-56insGT	ENSP00000362805.3:n.699-57_699-56insGT
ENST00000373719.7:c.729-57_729-56insGT	ENSP00000362824.3:n.729-57_729-56insGT
ENST00000455587.3:n.608-57_608-56insGT
ENST00000459760.1:n.106-57_106-56insGT
ENST00000488174.5:n.4165+541_4165+542insGT
NM_181672.2:c.729-57_729-56insGT	NP_858058.1:n.729-57_729-56insGT
NM_181673.2:c.699-57_699-56insGT	NP_858059.1:n.699-57_699-56insGT
XM_005262308.1:c.-220+541_-220+542insGT	XP_005262365.1:n.-220+541_-220+542insGT
XM_017029908.1:c.-220+541_-220+542insGT	XP_016885397.1:n.-220+541_-220+542insGT
XM_024452467.1:c.-220+541_-220+542insGT	XP_024308235.1:n.-220+541_-220+542insGT
NM_181672.3:c.729-57_729-56insGT MANE Select	NP_858058.1:n.729-57_729-56insGT
NM_181673.3:c.699-57_699-56insGT	NP_858059.1:n.699-57_699-56insGT