Canonical Allele Identifier: CA2694055064

Gene: OGT

Linked Data

• gnomAD v4: X-71555137-TGTGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555138_71555142del , CM000685.2:g.71555138_71555142del	GRCh38
NC_000023.10:g.70774988_70774992del , CM000685.1:g.70774988_70774992del	GRCh37
NC_000023.9:g.70691713_70691717del	NCBI36
NG_015875.1:g.27077_27081del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-52_660-48del	ENSP00000514559.1:n.660-52_660-48del
ENST00000699750.1:c.*588-52_*588-48del	ENSP00000514560.1:n.*588-52_*588-48del
ENST00000699751.1:n.1278+546_1278+550del
ENST00000699779.1:c.*3597-52_*3597-48del	ENSP00000514585.1:n.*3597-52_*3597-48del
ENST00000699780.1:c.728+546_728+550del	ENSP00000514586.1:n.728+546_728+550del
ENST00000699781.1:c.*332+546_*332+550del	ENSP00000514587.1:n.*332+546_*332+550del
ENST00000699782.1:c.630-52_630-48del	ENSP00000514588.1:n.630-52_630-48del
ENST00000699783.1:c.699-52_699-48del	ENSP00000514589.1:n.699-52_699-48del
ENST00000699784.1:c.699-52_699-48del	ENSP00000514590.1:n.699-52_699-48del
ENST00000699785.1:c.*734-52_*734-48del	ENSP00000514591.1:n.*734-52_*734-48del
ENST00000373719.8:c.729-52_729-48del MANE Select	ENSP00000362824.3:n.729-52_729-48del
ENST00000373701.7:c.699-52_699-48del	ENSP00000362805.3:n.699-52_699-48del
ENST00000373719.7:c.729-52_729-48del	ENSP00000362824.3:n.729-52_729-48del
ENST00000455587.3:n.608-52_608-48del
ENST00000459760.1:n.106-52_106-48del
ENST00000488174.5:n.4165+546_4165+550del
NM_181672.2:c.729-52_729-48del	NP_858058.1:n.729-52_729-48del
NM_181673.2:c.699-52_699-48del	NP_858059.1:n.699-52_699-48del
XM_005262308.1:c.-220+546_-220+550del	XP_005262365.1:n.-220+546_-220+550del
XM_017029908.1:c.-220+546_-220+550del	XP_016885397.1:n.-220+546_-220+550del
XM_024452467.1:c.-220+546_-220+550del	XP_024308235.1:n.-220+546_-220+550del
NM_181672.3:c.729-52_729-48del MANE Select	NP_858058.1:n.729-52_729-48del
NM_181673.3:c.699-52_699-48del	NP_858059.1:n.699-52_699-48del