Canonical Allele Identifier: CA413544975

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775041G>A (hg19) ; chrX:g.71555191G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555191G>A , CM000685.2:g.71555191G>A	GRCh38
NC_000023.10:g.70775041G>A , CM000685.1:g.70775041G>A	GRCh37
NC_000023.9:g.70691766G>A	NCBI36
NG_015875.1:g.27130G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.661G>A	ENSP00000514559.1:p.Ala221Thr
ENST00000699750.1:c.*589G>A	ENSP00000514560.1:n.*589G>A
ENST00000699751.1:n.1278+599G>A
ENST00000699779.1:c.*3598G>A	ENSP00000514585.1:n.*3598G>A
ENST00000699780.1:c.728+599G>A	ENSP00000514586.1:n.728+599G>A
ENST00000699781.1:c.*332+599G>A	ENSP00000514587.1:n.*332+599G>A
ENST00000699782.1:c.631G>A	ENSP00000514588.1:p.Ala211Thr
ENST00000699783.1:c.700G>A	ENSP00000514589.1:p.Ala234Thr
ENST00000699784.1:c.700G>A	ENSP00000514590.1:p.Ala234Thr
ENST00000699785.1:c.*735G>A	ENSP00000514591.1:n.*735G>A
ENST00000373719.8:c.730G>A MANE Select	ENSP00000362824.3:p.Ala244Thr
ENST00000373701.7:c.700G>A	ENSP00000362805.3:p.Ala234Thr
ENST00000373719.7:c.730G>A	ENSP00000362824.3:p.Ala244Thr
ENST00000455587.3:n.609G>A
ENST00000459760.1:n.107G>A
ENST00000488174.5:n.4165+599G>A
NM_181672.2:c.730G>A	NP_858058.1:p.Ala244Thr
NM_181673.2:c.700G>A	NP_858059.1:p.Ala234Thr
XM_005262308.1:c.-220+599G>A	XP_005262365.1:n.-220+599G>A
XM_017029908.1:c.-220+599G>A	XP_016885397.1:n.-220+599G>A
XM_024452467.1:c.-220+599G>A	XP_024308235.1:n.-220+599G>A
NM_181672.3:c.730G>A MANE Select	NP_858058.1:p.Ala244Thr
NM_181673.3:c.700G>A	NP_858059.1:p.Ala234Thr