Canonical Allele Identifier: CA10447586

Gene: OGT

Linked Data

• dbSNP Id: rs777170010
• ExAC: X:70775016 G / GTA
• MyVariant Identifiers: chrX:g.70775016_70775017insTA (hg19) ; chrX:g.71555166_71555167insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555167_71555168insAT , CM000685.2:g.71555167_71555168insAT	GRCh38
NC_000023.10:g.70775017_70775018insAT , CM000685.1:g.70775017_70775018insAT	GRCh37
NC_000023.9:g.70691742_70691743insAT	NCBI36
NG_015875.1:g.27106_27107insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-23_660-22insAT	ENSP00000514559.1:n.660-23_660-22insAT
ENST00000699750.1:c.*588-23_*588-22insAT	ENSP00000514560.1:n.*588-23_*588-22insAT
ENST00000699751.1:n.1278+575_1278+576insAT
ENST00000699779.1:c.*3597-23_*3597-22insAT	ENSP00000514585.1:n.*3597-23_*3597-22insAT
ENST00000699780.1:c.728+575_728+576insAT	ENSP00000514586.1:n.728+575_728+576insAT
ENST00000699781.1:c.*332+575_*332+576insAT	ENSP00000514587.1:n.*332+575_*332+576insAT
ENST00000699782.1:c.630-23_630-22insAT	ENSP00000514588.1:n.630-23_630-22insAT
ENST00000699783.1:c.699-23_699-22insAT	ENSP00000514589.1:n.699-23_699-22insAT
ENST00000699784.1:c.699-23_699-22insAT	ENSP00000514590.1:n.699-23_699-22insAT
ENST00000699785.1:c.*734-23_*734-22insAT	ENSP00000514591.1:n.*734-23_*734-22insAT
ENST00000373719.8:c.729-23_729-22insAT MANE Select	ENSP00000362824.3:n.729-23_729-22insAT
ENST00000373701.7:c.699-23_699-22insAT	ENSP00000362805.3:n.699-23_699-22insAT
ENST00000373719.7:c.729-23_729-22insAT	ENSP00000362824.3:n.729-23_729-22insAT
ENST00000455587.3:n.608-23_608-22insAT
ENST00000459760.1:n.106-23_106-22insAT
ENST00000488174.5:n.4165+575_4165+576insAT
NM_181672.2:c.729-23_729-22insAT	NP_858058.1:n.729-23_729-22insAT
NM_181673.2:c.699-23_699-22insAT	NP_858059.1:n.699-23_699-22insAT
XM_005262308.1:c.-220+575_-220+576insAT	XP_005262365.1:n.-220+575_-220+576insAT
XM_017029908.1:c.-220+575_-220+576insAT	XP_016885397.1:n.-220+575_-220+576insAT
XM_024452467.1:c.-220+575_-220+576insAT	XP_024308235.1:n.-220+575_-220+576insAT
NM_181672.3:c.729-23_729-22insAT MANE Select	NP_858058.1:n.729-23_729-22insAT
NM_181673.3:c.699-23_699-22insAT	NP_858059.1:n.699-23_699-22insAT