Canonical Allele Identifier: CA641958813

Gene: OGT

Linked Data

• dbSNP Id: rs1185478496
• gnomAD v2: X-70775007-T-TGC
• MyVariant Identifiers: chrX:g.70775007_70775008insGC (hg19) ; chrX:g.71555157_71555158insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555158_71555159insCG , CM000685.2:g.71555158_71555159insCG	GRCh38
NC_000023.10:g.70775008_70775009insCG , CM000685.1:g.70775008_70775009insCG	GRCh37
NC_000023.9:g.70691733_70691734insCG	NCBI36
NG_015875.1:g.27097_27098insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-32_660-31insCG	ENSP00000514559.1:n.660-32_660-31insCG
ENST00000699750.1:c.*588-32_*588-31insCG	ENSP00000514560.1:n.*588-32_*588-31insCG
ENST00000699751.1:n.1278+566_1278+567insCG
ENST00000699779.1:c.*3597-32_*3597-31insCG	ENSP00000514585.1:n.*3597-32_*3597-31insCG
ENST00000699780.1:c.728+566_728+567insCG	ENSP00000514586.1:n.728+566_728+567insCG
ENST00000699781.1:c.*332+566_*332+567insCG	ENSP00000514587.1:n.*332+566_*332+567insCG
ENST00000699782.1:c.630-32_630-31insCG	ENSP00000514588.1:n.630-32_630-31insCG
ENST00000699783.1:c.699-32_699-31insCG	ENSP00000514589.1:n.699-32_699-31insCG
ENST00000699784.1:c.699-32_699-31insCG	ENSP00000514590.1:n.699-32_699-31insCG
ENST00000699785.1:c.*734-32_*734-31insCG	ENSP00000514591.1:n.*734-32_*734-31insCG
ENST00000373719.8:c.729-32_729-31insCG MANE Select	ENSP00000362824.3:n.729-32_729-31insCG
ENST00000373701.7:c.699-32_699-31insCG	ENSP00000362805.3:n.699-32_699-31insCG
ENST00000373719.7:c.729-32_729-31insCG	ENSP00000362824.3:n.729-32_729-31insCG
ENST00000455587.3:n.608-32_608-31insCG
ENST00000459760.1:n.106-32_106-31insCG
ENST00000488174.5:n.4165+566_4165+567insCG
NM_181672.2:c.729-32_729-31insCG	NP_858058.1:n.729-32_729-31insCG
NM_181673.2:c.699-32_699-31insCG	NP_858059.1:n.699-32_699-31insCG
XM_005262308.1:c.-220+566_-220+567insCG	XP_005262365.1:n.-220+566_-220+567insCG
XM_017029908.1:c.-220+566_-220+567insCG	XP_016885397.1:n.-220+566_-220+567insCG
XM_024452467.1:c.-220+566_-220+567insCG	XP_024308235.1:n.-220+566_-220+567insCG
NM_181672.3:c.729-32_729-31insCG MANE Select	NP_858058.1:n.729-32_729-31insCG
NM_181673.3:c.699-32_699-31insCG	NP_858059.1:n.699-32_699-31insCG