Canonical Allele Identifier: CA2694055049

Gene: OGT

Linked Data

• gnomAD v4: X-71555131-ATTTTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555133_71555137del , CM000685.2:g.71555133_71555137del	GRCh38
NC_000023.10:g.70774983_70774987del , CM000685.1:g.70774983_70774987del	GRCh37
NC_000023.9:g.70691708_70691712del	NCBI36
NG_015875.1:g.27072_27076del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-57_660-53del	ENSP00000514559.1:n.660-57_660-53del
ENST00000699750.1:c.*588-57_*588-53del	ENSP00000514560.1:n.*588-57_*588-53del
ENST00000699751.1:n.1278+541_1278+545del
ENST00000699779.1:c.*3597-57_*3597-53del	ENSP00000514585.1:n.*3597-57_*3597-53del
ENST00000699780.1:c.728+541_728+545del	ENSP00000514586.1:n.728+541_728+545del
ENST00000699781.1:c.*332+541_*332+545del	ENSP00000514587.1:n.*332+541_*332+545del
ENST00000699782.1:c.630-57_630-53del	ENSP00000514588.1:n.630-57_630-53del
ENST00000699783.1:c.699-57_699-53del	ENSP00000514589.1:n.699-57_699-53del
ENST00000699784.1:c.699-57_699-53del	ENSP00000514590.1:n.699-57_699-53del
ENST00000699785.1:c.*734-57_*734-53del	ENSP00000514591.1:n.*734-57_*734-53del
ENST00000373719.8:c.729-57_729-53del MANE Select	ENSP00000362824.3:n.729-57_729-53del
ENST00000373701.7:c.699-57_699-53del	ENSP00000362805.3:n.699-57_699-53del
ENST00000373719.7:c.729-57_729-53del	ENSP00000362824.3:n.729-57_729-53del
ENST00000455587.3:n.608-57_608-53del
ENST00000459760.1:n.106-57_106-53del
ENST00000488174.5:n.4165+541_4165+545del
NM_181672.2:c.729-57_729-53del	NP_858058.1:n.729-57_729-53del
NM_181673.2:c.699-57_699-53del	NP_858059.1:n.699-57_699-53del
XM_005262308.1:c.-220+541_-220+545del	XP_005262365.1:n.-220+541_-220+545del
XM_017029908.1:c.-220+541_-220+545del	XP_016885397.1:n.-220+541_-220+545del
XM_024452467.1:c.-220+541_-220+545del	XP_024308235.1:n.-220+541_-220+545del
NM_181672.3:c.729-57_729-53del MANE Select	NP_858058.1:n.729-57_729-53del
NM_181673.3:c.699-57_699-53del	NP_858059.1:n.699-57_699-53del