Canonical Allele Identifier: CA877838329

Gene: OGT

Linked Data

• dbSNP Id: rs541950947
• gnomAD v3: X-71555134-T-TTTG
• gnomAD v4: X-71555134-T-TTTG
• MyVariant Identifiers: chrX:g.70774984_70774985insTTG (hg19) ; chrX:g.71555134_71555135insTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555135_71555136insTGT , CM000685.2:g.71555135_71555136insTGT	GRCh38
NC_000023.10:g.70774985_70774986insTGT , CM000685.1:g.70774985_70774986insTGT	GRCh37
NC_000023.9:g.70691710_70691711insTGT	NCBI36
NG_015875.1:g.27074_27075insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-55_660-54insTGT	ENSP00000514559.1:n.660-55_660-54insTGT
ENST00000699750.1:c.*588-55_*588-54insTGT	ENSP00000514560.1:n.*588-55_*588-54insTGT
ENST00000699751.1:n.1278+543_1278+544insTGT
ENST00000699779.1:c.*3597-55_*3597-54insTGT	ENSP00000514585.1:n.*3597-55_*3597-54insTGT
ENST00000699780.1:c.728+543_728+544insTGT	ENSP00000514586.1:n.728+543_728+544insTGT
ENST00000699781.1:c.*332+543_*332+544insTGT	ENSP00000514587.1:n.*332+543_*332+544insTGT
ENST00000699782.1:c.630-55_630-54insTGT	ENSP00000514588.1:n.630-55_630-54insTGT
ENST00000699783.1:c.699-55_699-54insTGT	ENSP00000514589.1:n.699-55_699-54insTGT
ENST00000699784.1:c.699-55_699-54insTGT	ENSP00000514590.1:n.699-55_699-54insTGT
ENST00000699785.1:c.*734-55_*734-54insTGT	ENSP00000514591.1:n.*734-55_*734-54insTGT
ENST00000373719.8:c.729-55_729-54insTGT MANE Select	ENSP00000362824.3:n.729-55_729-54insTGT
ENST00000373701.7:c.699-55_699-54insTGT	ENSP00000362805.3:n.699-55_699-54insTGT
ENST00000373719.7:c.729-55_729-54insTGT	ENSP00000362824.3:n.729-55_729-54insTGT
ENST00000455587.3:n.608-55_608-54insTGT
ENST00000459760.1:n.106-55_106-54insTGT
ENST00000488174.5:n.4165+543_4165+544insTGT
NM_181672.2:c.729-55_729-54insTGT	NP_858058.1:n.729-55_729-54insTGT
NM_181673.2:c.699-55_699-54insTGT	NP_858059.1:n.699-55_699-54insTGT
XM_005262308.1:c.-220+543_-220+544insTGT	XP_005262365.1:n.-220+543_-220+544insTGT
XM_017029908.1:c.-220+543_-220+544insTGT	XP_016885397.1:n.-220+543_-220+544insTGT
XM_024452467.1:c.-220+543_-220+544insTGT	XP_024308235.1:n.-220+543_-220+544insTGT
NM_181672.3:c.729-55_729-54insTGT MANE Select	NP_858058.1:n.729-55_729-54insTGT
NM_181673.3:c.699-55_699-54insTGT	NP_858059.1:n.699-55_699-54insTGT