Canonical Allele Identifier: CA331037730

Gene: OGT

Linked Data

• dbSNP Id: rs376605851
• gnomAD v2: X-70774984-T-TTGTG
• gnomAD v3: X-71555134-T-TTGTG
• gnomAD v4: X-71555134-T-TTGTG
• MyVariant Identifiers: chrX:g.70775029_70775030insGTGT (hg19) ; chrX:g.70774990_70774991insTGTG (hg19) ; chrX:g.70774988_70774989insTGTG (hg19) ; chrX:g.70774984_70774985insTGTG (hg19) ; chrX:g.71555179_71555180insGTGT (hg38) ; chrX:g.71555138_71555139insTGTG (hg38) ; chrX:g.71555134_71555135insTGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555176_71555179dup , CM000685.2:g.71555176_71555179dup	GRCh38
NC_000023.10:g.70775026_70775029dup , CM000685.1:g.70775026_70775029dup	GRCh37
NC_000023.9:g.70691751_70691754dup	NCBI36
NG_015875.1:g.27115_27118dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-14_660-11dup	ENSP00000514559.1:n.660-14_660-11dup
ENST00000699750.1:c.*588-14_*588-11dup	ENSP00000514560.1:n.*588-14_*588-11dup
ENST00000699751.1:n.1278+584_1278+587dup
ENST00000699779.1:c.*3597-14_*3597-11dup	ENSP00000514585.1:n.*3597-14_*3597-11dup
ENST00000699780.1:c.728+584_728+587dup	ENSP00000514586.1:n.728+584_728+587dup
ENST00000699781.1:c.*332+584_*332+587dup	ENSP00000514587.1:n.*332+584_*332+587dup
ENST00000699782.1:c.630-14_630-11dup	ENSP00000514588.1:n.630-14_630-11dup
ENST00000699783.1:c.699-14_699-11dup	ENSP00000514589.1:n.699-14_699-11dup
ENST00000699784.1:c.699-14_699-11dup	ENSP00000514590.1:n.699-14_699-11dup
ENST00000699785.1:c.*734-14_*734-11dup	ENSP00000514591.1:n.*734-14_*734-11dup
ENST00000373719.8:c.729-14_729-11dup MANE Select	ENSP00000362824.3:n.729-14_729-11dup
ENST00000373701.7:c.699-14_699-11dup	ENSP00000362805.3:n.699-14_699-11dup
ENST00000373719.7:c.729-14_729-11dup	ENSP00000362824.3:n.729-14_729-11dup
ENST00000455587.3:n.608-14_608-11dup
ENST00000459760.1:n.106-14_106-11dup
ENST00000488174.5:n.4165+584_4165+587dup
NM_181672.2:c.729-14_729-11dup	NP_858058.1:n.729-14_729-11dup
NM_181673.2:c.699-14_699-11dup	NP_858059.1:n.699-14_699-11dup
XM_005262308.1:c.-220+584_-220+587dup	XP_005262365.1:n.-220+584_-220+587dup
XM_017029908.1:c.-220+584_-220+587dup	XP_016885397.1:n.-220+584_-220+587dup
XM_024452467.1:c.-220+584_-220+587dup	XP_024308235.1:n.-220+584_-220+587dup
NM_181672.3:c.729-14_729-11dup MANE Select	NP_858058.1:n.729-14_729-11dup
NM_181673.3:c.699-14_699-11dup	NP_858059.1:n.699-14_699-11dup