Canonical Allele Identifier: CA413546088

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775161C>T (hg19) ; chrX:g.71555311C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555311C>T , CM000685.2:g.71555311C>T	GRCh38
NC_000023.10:g.70775161C>T , CM000685.1:g.70775161C>T	GRCh37
NC_000023.9:g.70691886C>T	NCBI36
NG_015875.1:g.27250C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.781C>T	ENSP00000514559.1:p.Arg261Trp
ENST00000699750.1:c.*709C>T	ENSP00000514560.1:n.*709C>T
ENST00000699751.1:n.1278+719C>T
ENST00000699779.1:c.*3718C>T	ENSP00000514585.1:n.*3718C>T
ENST00000699780.1:c.729-643C>T	ENSP00000514586.1:n.729-643C>T
ENST00000699781.1:c.*333-643C>T	ENSP00000514587.1:n.*333-643C>T
ENST00000699782.1:c.751C>T	ENSP00000514588.1:p.Arg251Trp
ENST00000699783.1:c.820C>T	ENSP00000514589.1:p.Arg274Trp
ENST00000699784.1:c.820C>T	ENSP00000514590.1:p.Arg274Trp
ENST00000699785.1:c.*855C>T	ENSP00000514591.1:n.*855C>T
ENST00000373719.8:c.850C>T MANE Select	ENSP00000362824.3:p.Arg284Trp
ENST00000373701.7:c.820C>T	ENSP00000362805.3:p.Arg274Trp
ENST00000373719.7:c.850C>T	ENSP00000362824.3:p.Arg284Trp
ENST00000459760.1:n.227C>T
ENST00000488174.5:n.4166-643C>T
NM_181672.2:c.850C>T	NP_858058.1:p.Arg284Trp
NM_181673.2:c.820C>T	NP_858059.1:p.Arg274Trp
XM_005262308.1:c.-219-643C>T	XP_005262365.1:n.-219-643C>T
XM_017029908.1:c.-219-643C>T	XP_016885397.1:n.-219-643C>T
XM_024452467.1:c.-219-643C>T	XP_024308235.1:n.-219-643C>T
NM_181672.3:c.850C>T MANE Select	NP_858058.1:p.Arg284Trp
NM_181673.3:c.820C>T	NP_858059.1:p.Arg274Trp