Canonical Allele Identifier: CA413545442

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775095C>A (hg19) ; chrX:g.71555245C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555245C>A , CM000685.2:g.71555245C>A	GRCh38
NC_000023.10:g.70775095C>A , CM000685.1:g.70775095C>A	GRCh37
NC_000023.9:g.70691820C>A	NCBI36
NG_015875.1:g.27184C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.715C>A	ENSP00000514559.1:p.His239Asn
ENST00000699750.1:c.*643C>A	ENSP00000514560.1:n.*643C>A
ENST00000699751.1:n.1278+653C>A
ENST00000699779.1:c.*3652C>A	ENSP00000514585.1:n.*3652C>A
ENST00000699780.1:c.728+653C>A	ENSP00000514586.1:n.728+653C>A
ENST00000699781.1:c.*332+653C>A	ENSP00000514587.1:n.*332+653C>A
ENST00000699782.1:c.685C>A	ENSP00000514588.1:p.His229Asn
ENST00000699783.1:c.754C>A	ENSP00000514589.1:p.His252Asn
ENST00000699784.1:c.754C>A	ENSP00000514590.1:p.His252Asn
ENST00000699785.1:c.*789C>A	ENSP00000514591.1:n.*789C>A
ENST00000373719.8:c.784C>A MANE Select	ENSP00000362824.3:p.His262Asn
ENST00000373701.7:c.754C>A	ENSP00000362805.3:p.His252Asn
ENST00000373719.7:c.784C>A	ENSP00000362824.3:p.His262Asn
ENST00000459760.1:n.161C>A
ENST00000488174.5:n.4165+653C>A
NM_181672.2:c.784C>A	NP_858058.1:p.His262Asn
NM_181673.2:c.754C>A	NP_858059.1:p.His252Asn
XM_005262308.1:c.-220+653C>A	XP_005262365.1:n.-220+653C>A
XM_017029908.1:c.-220+653C>A	XP_016885397.1:n.-220+653C>A
XM_024452467.1:c.-220+653C>A	XP_024308235.1:n.-220+653C>A
NM_181672.3:c.784C>A MANE Select	NP_858058.1:p.His262Asn
NM_181673.3:c.754C>A	NP_858059.1:p.His252Asn