Canonical Allele Identifier: CA2821740607

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555139_71555140insATGT , CM000685.2:g.71555139_71555140insATGT	GRCh38
NC_000023.10:g.70774989_70774990insATGT , CM000685.1:g.70774989_70774990insATGT	GRCh37
NC_000023.9:g.70691714_70691715insATGT	NCBI36
NG_015875.1:g.27078_27079insATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-51_660-50insATGT	ENSP00000514559.1:n.660-51_660-50insATGT
ENST00000699750.1:c.*588-51_*588-50insATGT	ENSP00000514560.1:n.*588-51_*588-50insATGT
ENST00000699751.1:n.1278+547_1278+548insATGT
ENST00000699779.1:c.*3597-51_*3597-50insATGT	ENSP00000514585.1:n.*3597-51_*3597-50insATGT
ENST00000699780.1:c.728+547_728+548insATGT	ENSP00000514586.1:n.728+547_728+548insATGT
ENST00000699781.1:c.*332+547_*332+548insATGT	ENSP00000514587.1:n.*332+547_*332+548insATGT
ENST00000699782.1:c.630-51_630-50insATGT	ENSP00000514588.1:n.630-51_630-50insATGT
ENST00000699783.1:c.699-51_699-50insATGT	ENSP00000514589.1:n.699-51_699-50insATGT
ENST00000699784.1:c.699-51_699-50insATGT	ENSP00000514590.1:n.699-51_699-50insATGT
ENST00000699785.1:c.*734-51_*734-50insATGT	ENSP00000514591.1:n.*734-51_*734-50insATGT
ENST00000373719.8:c.729-51_729-50insATGT MANE Select	ENSP00000362824.3:n.729-51_729-50insATGT
ENST00000373701.7:c.699-51_699-50insATGT	ENSP00000362805.3:n.699-51_699-50insATGT
ENST00000373719.7:c.729-51_729-50insATGT	ENSP00000362824.3:n.729-51_729-50insATGT
ENST00000455587.3:n.608-51_608-50insATGT
ENST00000459760.1:n.106-51_106-50insATGT
ENST00000488174.5:n.4165+547_4165+548insATGT
NM_181672.2:c.729-51_729-50insATGT	NP_858058.1:n.729-51_729-50insATGT
NM_181673.2:c.699-51_699-50insATGT	NP_858059.1:n.699-51_699-50insATGT
XM_005262308.1:c.-220+547_-220+548insATGT	XP_005262365.1:n.-220+547_-220+548insATGT
XM_017029908.1:c.-220+547_-220+548insATGT	XP_016885397.1:n.-220+547_-220+548insATGT
XM_024452467.1:c.-220+547_-220+548insATGT	XP_024308235.1:n.-220+547_-220+548insATGT
NM_181672.3:c.729-51_729-50insATGT MANE Select	NP_858058.1:n.729-51_729-50insATGT
NM_181673.3:c.699-51_699-50insATGT	NP_858059.1:n.699-51_699-50insATGT