Canonical Allele Identifier: CA516728090

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775130C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555280C>T , CM000685.2:g.71555280C>T	GRCh38
NC_000023.10:g.70775130C>T , CM000685.1:g.70775130C>T	GRCh37
NC_000023.9:g.70691855C>T	NCBI36
NG_015875.1:g.27219C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.750C>T	ENSP00000514559.1:p.Gly250=
ENST00000699750.1:c.*678C>T	ENSP00000514560.1:n.*678C>T
ENST00000699751.1:n.1278+688C>T
ENST00000699779.1:c.*3687C>T	ENSP00000514585.1:n.*3687C>T
ENST00000699780.1:c.729-674C>T	ENSP00000514586.1:n.729-674C>T
ENST00000699781.1:c.*333-674C>T	ENSP00000514587.1:n.*333-674C>T
ENST00000699782.1:c.720C>T	ENSP00000514588.1:p.Gly240=
ENST00000699783.1:c.789C>T	ENSP00000514589.1:p.Gly263=
ENST00000699784.1:c.789C>T	ENSP00000514590.1:p.Gly263=
ENST00000699785.1:c.*824C>T	ENSP00000514591.1:n.*824C>T
ENST00000373719.8:c.819C>T MANE Select	ENSP00000362824.3:p.Gly273=
ENST00000373701.7:c.789C>T	ENSP00000362805.3:p.Gly263=
ENST00000373719.7:c.819C>T	ENSP00000362824.3:p.Gly273=
ENST00000459760.1:n.196C>T
ENST00000488174.5:n.4166-674C>T
NM_181672.2:c.819C>T	NP_858058.1:p.Gly273=
NM_181673.2:c.789C>T	NP_858059.1:p.Gly263=
XM_005262308.1:c.-219-674C>T	XP_005262365.1:n.-219-674C>T
XM_017029908.1:c.-219-674C>T	XP_016885397.1:n.-219-674C>T
XM_024452467.1:c.-219-674C>T	XP_024308235.1:n.-219-674C>T
NM_181672.3:c.819C>T MANE Select	NP_858058.1:p.Gly273=
NM_181673.3:c.789C>T	NP_858059.1:p.Gly263=