Canonical Allele Identifier: CA516727892

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775043T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555193T>G , CM000685.2:g.71555193T>G	GRCh38
NC_000023.10:g.70775043T>G , CM000685.1:g.70775043T>G	GRCh37
NC_000023.9:g.70691768T>G	NCBI36
NG_015875.1:g.27132T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.663T>G	ENSP00000514559.1:p.Ala221=
ENST00000699750.1:c.*591T>G	ENSP00000514560.1:n.*591T>G
ENST00000699751.1:n.1278+601T>G
ENST00000699779.1:c.*3600T>G	ENSP00000514585.1:n.*3600T>G
ENST00000699780.1:c.728+601T>G	ENSP00000514586.1:n.728+601T>G
ENST00000699781.1:c.*332+601T>G	ENSP00000514587.1:n.*332+601T>G
ENST00000699782.1:c.633T>G	ENSP00000514588.1:p.Ala211=
ENST00000699783.1:c.702T>G	ENSP00000514589.1:p.Ala234=
ENST00000699784.1:c.702T>G	ENSP00000514590.1:p.Ala234=
ENST00000699785.1:c.*737T>G	ENSP00000514591.1:n.*737T>G
ENST00000373719.8:c.732T>G MANE Select	ENSP00000362824.3:p.Ala244=
ENST00000373701.7:c.702T>G	ENSP00000362805.3:p.Ala234=
ENST00000373719.7:c.732T>G	ENSP00000362824.3:p.Ala244=
ENST00000455587.3:n.611T>G
ENST00000459760.1:n.109T>G
ENST00000488174.5:n.4165+601T>G
NM_181672.2:c.732T>G	NP_858058.1:p.Ala244=
NM_181673.2:c.702T>G	NP_858059.1:p.Ala234=
XM_005262308.1:c.-220+601T>G	XP_005262365.1:n.-220+601T>G
XM_017029908.1:c.-220+601T>G	XP_016885397.1:n.-220+601T>G
XM_024452467.1:c.-220+601T>G	XP_024308235.1:n.-220+601T>G
NM_181672.3:c.732T>G MANE Select	NP_858058.1:p.Ala244=
NM_181673.3:c.702T>G	NP_858059.1:p.Ala234=