Canonical Allele Identifier: CA2694055065

Gene: OGT

Linked Data

• gnomAD v4: X-71555141-T-TGC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555142_71555143insCG , CM000685.2:g.71555142_71555143insCG	GRCh38
NC_000023.10:g.70774992_70774993insCG , CM000685.1:g.70774992_70774993insCG	GRCh37
NC_000023.9:g.70691717_70691718insCG	NCBI36
NG_015875.1:g.27081_27082insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-48_660-47insCG	ENSP00000514559.1:n.660-48_660-47insCG
ENST00000699750.1:c.*588-48_*588-47insCG	ENSP00000514560.1:n.*588-48_*588-47insCG
ENST00000699751.1:n.1278+550_1278+551insCG
ENST00000699779.1:c.*3597-48_*3597-47insCG	ENSP00000514585.1:n.*3597-48_*3597-47insCG
ENST00000699780.1:c.728+550_728+551insCG	ENSP00000514586.1:n.728+550_728+551insCG
ENST00000699781.1:c.*332+550_*332+551insCG	ENSP00000514587.1:n.*332+550_*332+551insCG
ENST00000699782.1:c.630-48_630-47insCG	ENSP00000514588.1:n.630-48_630-47insCG
ENST00000699783.1:c.699-48_699-47insCG	ENSP00000514589.1:n.699-48_699-47insCG
ENST00000699784.1:c.699-48_699-47insCG	ENSP00000514590.1:n.699-48_699-47insCG
ENST00000699785.1:c.*734-48_*734-47insCG	ENSP00000514591.1:n.*734-48_*734-47insCG
ENST00000373719.8:c.729-48_729-47insCG MANE Select	ENSP00000362824.3:n.729-48_729-47insCG
ENST00000373701.7:c.699-48_699-47insCG	ENSP00000362805.3:n.699-48_699-47insCG
ENST00000373719.7:c.729-48_729-47insCG	ENSP00000362824.3:n.729-48_729-47insCG
ENST00000455587.3:n.608-48_608-47insCG
ENST00000459760.1:n.106-48_106-47insCG
ENST00000488174.5:n.4165+550_4165+551insCG
NM_181672.2:c.729-48_729-47insCG	NP_858058.1:n.729-48_729-47insCG
NM_181673.2:c.699-48_699-47insCG	NP_858059.1:n.699-48_699-47insCG
XM_005262308.1:c.-220+550_-220+551insCG	XP_005262365.1:n.-220+550_-220+551insCG
XM_017029908.1:c.-220+550_-220+551insCG	XP_016885397.1:n.-220+550_-220+551insCG
XM_024452467.1:c.-220+550_-220+551insCG	XP_024308235.1:n.-220+550_-220+551insCG
NM_181672.3:c.729-48_729-47insCG MANE Select	NP_858058.1:n.729-48_729-47insCG
NM_181673.3:c.699-48_699-47insCG	NP_858059.1:n.699-48_699-47insCG