Canonical Allele Identifier: CA413545436

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775093T>C (hg19) ; chrX:g.71555243T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555243T>C , CM000685.2:g.71555243T>C	GRCh38
NC_000023.10:g.70775093T>C , CM000685.1:g.70775093T>C	GRCh37
NC_000023.9:g.70691818T>C	NCBI36
NG_015875.1:g.27182T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.713T>C	ENSP00000514559.1:p.Val238Ala
ENST00000699750.1:c.*641T>C	ENSP00000514560.1:n.*641T>C
ENST00000699751.1:n.1278+651T>C
ENST00000699779.1:c.*3650T>C	ENSP00000514585.1:n.*3650T>C
ENST00000699780.1:c.728+651T>C	ENSP00000514586.1:n.728+651T>C
ENST00000699781.1:c.*332+651T>C	ENSP00000514587.1:n.*332+651T>C
ENST00000699782.1:c.683T>C	ENSP00000514588.1:p.Val228Ala
ENST00000699783.1:c.752T>C	ENSP00000514589.1:p.Val251Ala
ENST00000699784.1:c.752T>C	ENSP00000514590.1:p.Val251Ala
ENST00000699785.1:c.*787T>C	ENSP00000514591.1:n.*787T>C
ENST00000373719.8:c.782T>C MANE Select	ENSP00000362824.3:p.Val261Ala
ENST00000373701.7:c.752T>C	ENSP00000362805.3:p.Val251Ala
ENST00000373719.7:c.782T>C	ENSP00000362824.3:p.Val261Ala
ENST00000459760.1:n.159T>C
ENST00000488174.5:n.4165+651T>C
NM_181672.2:c.782T>C	NP_858058.1:p.Val261Ala
NM_181673.2:c.752T>C	NP_858059.1:p.Val251Ala
XM_005262308.1:c.-220+651T>C	XP_005262365.1:n.-220+651T>C
XM_017029908.1:c.-220+651T>C	XP_016885397.1:n.-220+651T>C
XM_024452467.1:c.-220+651T>C	XP_024308235.1:n.-220+651T>C
NM_181672.3:c.782T>C MANE Select	NP_858058.1:p.Val261Ala
NM_181673.3:c.752T>C	NP_858059.1:p.Val251Ala