Canonical Allele Identifier: CA641958811

Gene: OGT

Linked Data

• dbSNP Id: rs1255695973
• gnomAD v2: X-70775001-T-TGC
• MyVariant Identifiers: chrX:g.70775001_70775002insGC (hg19) ; chrX:g.71555151_71555152insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555152_71555153insCG , CM000685.2:g.71555152_71555153insCG	GRCh38
NC_000023.10:g.70775002_70775003insCG , CM000685.1:g.70775002_70775003insCG	GRCh37
NC_000023.9:g.70691727_70691728insCG	NCBI36
NG_015875.1:g.27091_27092insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-38_660-37insCG	ENSP00000514559.1:n.660-38_660-37insCG
ENST00000699750.1:c.*588-38_*588-37insCG	ENSP00000514560.1:n.*588-38_*588-37insCG
ENST00000699751.1:n.1278+560_1278+561insCG
ENST00000699779.1:c.*3597-38_*3597-37insCG	ENSP00000514585.1:n.*3597-38_*3597-37insCG
ENST00000699780.1:c.728+560_728+561insCG	ENSP00000514586.1:n.728+560_728+561insCG
ENST00000699781.1:c.*332+560_*332+561insCG	ENSP00000514587.1:n.*332+560_*332+561insCG
ENST00000699782.1:c.630-38_630-37insCG	ENSP00000514588.1:n.630-38_630-37insCG
ENST00000699783.1:c.699-38_699-37insCG	ENSP00000514589.1:n.699-38_699-37insCG
ENST00000699784.1:c.699-38_699-37insCG	ENSP00000514590.1:n.699-38_699-37insCG
ENST00000699785.1:c.*734-38_*734-37insCG	ENSP00000514591.1:n.*734-38_*734-37insCG
ENST00000373719.8:c.729-38_729-37insCG MANE Select	ENSP00000362824.3:n.729-38_729-37insCG
ENST00000373701.7:c.699-38_699-37insCG	ENSP00000362805.3:n.699-38_699-37insCG
ENST00000373719.7:c.729-38_729-37insCG	ENSP00000362824.3:n.729-38_729-37insCG
ENST00000455587.3:n.608-38_608-37insCG
ENST00000459760.1:n.106-38_106-37insCG
ENST00000488174.5:n.4165+560_4165+561insCG
NM_181672.2:c.729-38_729-37insCG	NP_858058.1:n.729-38_729-37insCG
NM_181673.2:c.699-38_699-37insCG	NP_858059.1:n.699-38_699-37insCG
XM_005262308.1:c.-220+560_-220+561insCG	XP_005262365.1:n.-220+560_-220+561insCG
XM_017029908.1:c.-220+560_-220+561insCG	XP_016885397.1:n.-220+560_-220+561insCG
XM_024452467.1:c.-220+560_-220+561insCG	XP_024308235.1:n.-220+560_-220+561insCG
NM_181672.3:c.729-38_729-37insCG MANE Select	NP_858058.1:n.729-38_729-37insCG
NM_181673.3:c.699-38_699-37insCG	NP_858059.1:n.699-38_699-37insCG