Canonical Allele Identifier: CA2694055100

Gene: OGT

Linked Data

• gnomAD v4: X-71555170-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555171_71555172insCT , CM000685.2:g.71555171_71555172insCT	GRCh38
NC_000023.10:g.70775021_70775022insCT , CM000685.1:g.70775021_70775022insCT	GRCh37
NC_000023.9:g.70691746_70691747insCT	NCBI36
NG_015875.1:g.27110_27111insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-19_660-18insCT	ENSP00000514559.1:n.660-19_660-18insCT
ENST00000699750.1:c.*588-19_*588-18insCT	ENSP00000514560.1:n.*588-19_*588-18insCT
ENST00000699751.1:n.1278+579_1278+580insCT
ENST00000699779.1:c.*3597-19_*3597-18insCT	ENSP00000514585.1:n.*3597-19_*3597-18insCT
ENST00000699780.1:c.728+579_728+580insCT	ENSP00000514586.1:n.728+579_728+580insCT
ENST00000699781.1:c.*332+579_*332+580insCT	ENSP00000514587.1:n.*332+579_*332+580insCT
ENST00000699782.1:c.630-19_630-18insCT	ENSP00000514588.1:n.630-19_630-18insCT
ENST00000699783.1:c.699-19_699-18insCT	ENSP00000514589.1:n.699-19_699-18insCT
ENST00000699784.1:c.699-19_699-18insCT	ENSP00000514590.1:n.699-19_699-18insCT
ENST00000699785.1:c.*734-19_*734-18insCT	ENSP00000514591.1:n.*734-19_*734-18insCT
ENST00000373719.8:c.729-19_729-18insCT MANE Select	ENSP00000362824.3:n.729-19_729-18insCT
ENST00000373701.7:c.699-19_699-18insCT	ENSP00000362805.3:n.699-19_699-18insCT
ENST00000373719.7:c.729-19_729-18insCT	ENSP00000362824.3:n.729-19_729-18insCT
ENST00000455587.3:n.608-19_608-18insCT
ENST00000459760.1:n.106-19_106-18insCT
ENST00000488174.5:n.4165+579_4165+580insCT
NM_181672.2:c.729-19_729-18insCT	NP_858058.1:n.729-19_729-18insCT
NM_181673.2:c.699-19_699-18insCT	NP_858059.1:n.699-19_699-18insCT
XM_005262308.1:c.-220+579_-220+580insCT	XP_005262365.1:n.-220+579_-220+580insCT
XM_017029908.1:c.-220+579_-220+580insCT	XP_016885397.1:n.-220+579_-220+580insCT
XM_024452467.1:c.-220+579_-220+580insCT	XP_024308235.1:n.-220+579_-220+580insCT
NM_181672.3:c.729-19_729-18insCT MANE Select	NP_858058.1:n.729-19_729-18insCT
NM_181673.3:c.699-19_699-18insCT	NP_858059.1:n.699-19_699-18insCT