Canonical Allele Identifier: CA413545700

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775123A>C (hg19) ; chrX:g.71555273A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555273A>C , CM000685.2:g.71555273A>C	GRCh38
NC_000023.10:g.70775123A>C , CM000685.1:g.70775123A>C	GRCh37
NC_000023.9:g.70691848A>C	NCBI36
NG_015875.1:g.27212A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.743A>C	ENSP00000514559.1:p.Glu248Ala
ENST00000699750.1:c.*671A>C	ENSP00000514560.1:n.*671A>C
ENST00000699751.1:n.1278+681A>C
ENST00000699779.1:c.*3680A>C	ENSP00000514585.1:n.*3680A>C
ENST00000699780.1:c.729-681A>C	ENSP00000514586.1:n.729-681A>C
ENST00000699781.1:c.*333-681A>C	ENSP00000514587.1:n.*333-681A>C
ENST00000699782.1:c.713A>C	ENSP00000514588.1:p.Glu238Ala
ENST00000699783.1:c.782A>C	ENSP00000514589.1:p.Glu261Ala
ENST00000699784.1:c.782A>C	ENSP00000514590.1:p.Glu261Ala
ENST00000699785.1:c.*817A>C	ENSP00000514591.1:n.*817A>C
ENST00000373719.8:c.812A>C MANE Select	ENSP00000362824.3:p.Glu271Ala
ENST00000373701.7:c.782A>C	ENSP00000362805.3:p.Glu261Ala
ENST00000373719.7:c.812A>C	ENSP00000362824.3:p.Glu271Ala
ENST00000459760.1:n.189A>C
ENST00000488174.5:n.4166-681A>C
NM_181672.2:c.812A>C	NP_858058.1:p.Glu271Ala
NM_181673.2:c.782A>C	NP_858059.1:p.Glu261Ala
XM_005262308.1:c.-219-681A>C	XP_005262365.1:n.-219-681A>C
XM_017029908.1:c.-219-681A>C	XP_016885397.1:n.-219-681A>C
XM_024452467.1:c.-219-681A>C	XP_024308235.1:n.-219-681A>C
NM_181672.3:c.812A>C MANE Select	NP_858058.1:p.Glu271Ala
NM_181673.3:c.782A>C	NP_858059.1:p.Glu261Ala