Canonical Allele Identifier: CA10447588

Gene: OGT

Linked Data

• dbSNP Id: rs769409272
• ExAC: X:70775023 T / TGC
• MyVariant Identifiers: chrX:g.70775023_70775024insGC (hg19) ; chrX:g.71555173_71555174insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555174_71555175insCG , CM000685.2:g.71555174_71555175insCG	GRCh38
NC_000023.10:g.70775024_70775025insCG , CM000685.1:g.70775024_70775025insCG	GRCh37
NC_000023.9:g.70691749_70691750insCG	NCBI36
NG_015875.1:g.27113_27114insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-16_660-15insCG	ENSP00000514559.1:n.660-16_660-15insCG
ENST00000699750.1:c.*588-16_*588-15insCG	ENSP00000514560.1:n.*588-16_*588-15insCG
ENST00000699751.1:n.1278+582_1278+583insCG
ENST00000699779.1:c.*3597-16_*3597-15insCG	ENSP00000514585.1:n.*3597-16_*3597-15insCG
ENST00000699780.1:c.728+582_728+583insCG	ENSP00000514586.1:n.728+582_728+583insCG
ENST00000699781.1:c.*332+582_*332+583insCG	ENSP00000514587.1:n.*332+582_*332+583insCG
ENST00000699782.1:c.630-16_630-15insCG	ENSP00000514588.1:n.630-16_630-15insCG
ENST00000699783.1:c.699-16_699-15insCG	ENSP00000514589.1:n.699-16_699-15insCG
ENST00000699784.1:c.699-16_699-15insCG	ENSP00000514590.1:n.699-16_699-15insCG
ENST00000699785.1:c.*734-16_*734-15insCG	ENSP00000514591.1:n.*734-16_*734-15insCG
ENST00000373719.8:c.729-16_729-15insCG MANE Select	ENSP00000362824.3:n.729-16_729-15insCG
ENST00000373701.7:c.699-16_699-15insCG	ENSP00000362805.3:n.699-16_699-15insCG
ENST00000373719.7:c.729-16_729-15insCG	ENSP00000362824.3:n.729-16_729-15insCG
ENST00000455587.3:n.608-16_608-15insCG
ENST00000459760.1:n.106-16_106-15insCG
ENST00000488174.5:n.4165+582_4165+583insCG
NM_181672.2:c.729-16_729-15insCG	NP_858058.1:n.729-16_729-15insCG
NM_181673.2:c.699-16_699-15insCG	NP_858059.1:n.699-16_699-15insCG
XM_005262308.1:c.-220+582_-220+583insCG	XP_005262365.1:n.-220+582_-220+583insCG
XM_017029908.1:c.-220+582_-220+583insCG	XP_016885397.1:n.-220+582_-220+583insCG
XM_024452467.1:c.-220+582_-220+583insCG	XP_024308235.1:n.-220+582_-220+583insCG
NM_181672.3:c.729-16_729-15insCG MANE Select	NP_858058.1:n.729-16_729-15insCG
NM_181673.3:c.699-16_699-15insCG	NP_858059.1:n.699-16_699-15insCG