Canonical Allele Identifier: CA2694055048

Gene: OGT

Linked Data

• gnomAD v4: X-71555131-ATTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555132_71555135del , CM000685.2:g.71555132_71555135del	GRCh38
NC_000023.10:g.70774982_70774985del , CM000685.1:g.70774982_70774985del	GRCh37
NC_000023.9:g.70691707_70691710del	NCBI36
NG_015875.1:g.27071_27074del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-58_660-55del	ENSP00000514559.1:n.660-58_660-55del
ENST00000699750.1:c.*588-58_*588-55del	ENSP00000514560.1:n.*588-58_*588-55del
ENST00000699751.1:n.1278+540_1278+543del
ENST00000699779.1:c.*3597-58_*3597-55del	ENSP00000514585.1:n.*3597-58_*3597-55del
ENST00000699780.1:c.728+540_728+543del	ENSP00000514586.1:n.728+540_728+543del
ENST00000699781.1:c.*332+540_*332+543del	ENSP00000514587.1:n.*332+540_*332+543del
ENST00000699782.1:c.630-58_630-55del	ENSP00000514588.1:n.630-58_630-55del
ENST00000699783.1:c.699-58_699-55del	ENSP00000514589.1:n.699-58_699-55del
ENST00000699784.1:c.699-58_699-55del	ENSP00000514590.1:n.699-58_699-55del
ENST00000699785.1:c.*734-58_*734-55del	ENSP00000514591.1:n.*734-58_*734-55del
ENST00000373719.8:c.729-58_729-55del MANE Select	ENSP00000362824.3:n.729-58_729-55del
ENST00000373701.7:c.699-58_699-55del	ENSP00000362805.3:n.699-58_699-55del
ENST00000373719.7:c.729-58_729-55del	ENSP00000362824.3:n.729-58_729-55del
ENST00000455587.3:n.608-58_608-55del
ENST00000459760.1:n.106-58_106-55del
ENST00000488174.5:n.4165+540_4165+543del
NM_181672.2:c.729-58_729-55del	NP_858058.1:n.729-58_729-55del
NM_181673.2:c.699-58_699-55del	NP_858059.1:n.699-58_699-55del
XM_005262308.1:c.-220+540_-220+543del	XP_005262365.1:n.-220+540_-220+543del
XM_017029908.1:c.-220+540_-220+543del	XP_016885397.1:n.-220+540_-220+543del
XM_024452467.1:c.-220+540_-220+543del	XP_024308235.1:n.-220+540_-220+543del
NM_181672.3:c.729-58_729-55del MANE Select	NP_858058.1:n.729-58_729-55del
NM_181673.3:c.699-58_699-55del	NP_858059.1:n.699-58_699-55del