Canonical Allele Identifier: CA10447591

Gene: OGT

Linked Data

• dbSNP Id: rs59360802
• ExAC: X:70775029 T / TGTGTGTGTG
• gnomAD v2: X-70775029-T-TGTGTGTGTG
• gnomAD v3: X-71555179-T-TGTGTGTGTG
• gnomAD v4: X-71555179-T-TGTGTGTGTG
• MyVariant Identifiers: chrX:g.70775029_70775030insGTGTGTGTG (hg19) ; chrX:g.71555179_71555180insGTGTGTGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555179_71555180insGTGTGTGTG , CM000685.2:g.71555179_71555180insGTGTGTGTG	GRCh38
NC_000023.10:g.70775029_70775030insGTGTGTGTG , CM000685.1:g.70775029_70775030insGTGTGTGTG	GRCh37
NC_000023.9:g.70691754_70691755insGTGTGTGTG	NCBI36
NG_015875.1:g.27118_27119insGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-11_660-10insGTGTGTGTG	ENSP00000514559.1:n.660-11_660-10insGTGTGTGTG
ENST00000699750.1:c.*588-11_*588-10insGTGTGTGTG	ENSP00000514560.1:n.*588-11_*588-10insGTGTGTGTG
ENST00000699751.1:n.1278+587_1278+588insGTGTGTGTG
ENST00000699779.1:c.*3597-11_*3597-10insGTGTGTGTG	ENSP00000514585.1:n.*3597-11_*3597-10insGTGTGTGTG
ENST00000699780.1:c.728+587_728+588insGTGTGTGTG	ENSP00000514586.1:n.728+587_728+588insGTGTGTGTG
ENST00000699781.1:c.*332+587_*332+588insGTGTGTGTG	ENSP00000514587.1:n.*332+587_*332+588insGTGTGTGTG
ENST00000699782.1:c.630-11_630-10insGTGTGTGTG	ENSP00000514588.1:n.630-11_630-10insGTGTGTGTG
ENST00000699783.1:c.699-11_699-10insGTGTGTGTG	ENSP00000514589.1:n.699-11_699-10insGTGTGTGTG
ENST00000699784.1:c.699-11_699-10insGTGTGTGTG	ENSP00000514590.1:n.699-11_699-10insGTGTGTGTG
ENST00000699785.1:c.*734-11_*734-10insGTGTGTGTG	ENSP00000514591.1:n.*734-11_*734-10insGTGTGTGTG
ENST00000373719.8:c.729-11_729-10insGTGTGTGTG MANE Select	ENSP00000362824.3:n.729-11_729-10insGTGTGTGTG
ENST00000373701.7:c.699-11_699-10insGTGTGTGTG	ENSP00000362805.3:n.699-11_699-10insGTGTGTGTG
ENST00000373719.7:c.729-11_729-10insGTGTGTGTG	ENSP00000362824.3:n.729-11_729-10insGTGTGTGTG
ENST00000455587.3:n.608-11_608-10insGTGTGTGTG
ENST00000459760.1:n.106-11_106-10insGTGTGTGTG
ENST00000488174.5:n.4165+587_4165+588insGTGTGTGTG
NM_181672.2:c.729-11_729-10insGTGTGTGTG	NP_858058.1:n.729-11_729-10insGTGTGTGTG
NM_181673.2:c.699-11_699-10insGTGTGTGTG	NP_858059.1:n.699-11_699-10insGTGTGTGTG
XM_005262308.1:c.-220+587_-220+588insGTGTGTGTG	XP_005262365.1:n.-220+587_-220+588insGTGTGTGTG
XM_017029908.1:c.-220+587_-220+588insGTGTGTGTG	XP_016885397.1:n.-220+587_-220+588insGTGTGTGTG
XM_024452467.1:c.-220+587_-220+588insGTGTGTGTG	XP_024308235.1:n.-220+587_-220+588insGTGTGTGTG
NM_181672.3:c.729-11_729-10insGTGTGTGTG MANE Select	NP_858058.1:n.729-11_729-10insGTGTGTGTG
NM_181673.3:c.699-11_699-10insGTGTGTGTG	NP_858059.1:n.699-11_699-10insGTGTGTGTG