Canonical Allele Identifier: CA413545157

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775062G>A (hg19) ; chrX:g.71555212G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555212G>A , CM000685.2:g.71555212G>A	GRCh38
NC_000023.10:g.70775062G>A , CM000685.1:g.70775062G>A	GRCh37
NC_000023.9:g.70691787G>A	NCBI36
NG_015875.1:g.27151G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.682G>A	ENSP00000514559.1:p.Ala228Thr
ENST00000699750.1:c.*610G>A	ENSP00000514560.1:n.*610G>A
ENST00000699751.1:n.1278+620G>A
ENST00000699779.1:c.*3619G>A	ENSP00000514585.1:n.*3619G>A
ENST00000699780.1:c.728+620G>A	ENSP00000514586.1:n.728+620G>A
ENST00000699781.1:c.*332+620G>A	ENSP00000514587.1:n.*332+620G>A
ENST00000699782.1:c.652G>A	ENSP00000514588.1:p.Ala218Thr
ENST00000699783.1:c.721G>A	ENSP00000514589.1:p.Ala241Thr
ENST00000699784.1:c.721G>A	ENSP00000514590.1:p.Ala241Thr
ENST00000699785.1:c.*756G>A	ENSP00000514591.1:n.*756G>A
ENST00000373719.8:c.751G>A MANE Select	ENSP00000362824.3:p.Ala251Thr
ENST00000373701.7:c.721G>A	ENSP00000362805.3:p.Ala241Thr
ENST00000373719.7:c.751G>A	ENSP00000362824.3:p.Ala251Thr
ENST00000455587.3:n.630G>A
ENST00000459760.1:n.128G>A
ENST00000488174.5:n.4165+620G>A
NM_181672.2:c.751G>A	NP_858058.1:p.Ala251Thr
NM_181673.2:c.721G>A	NP_858059.1:p.Ala241Thr
XM_005262308.1:c.-220+620G>A	XP_005262365.1:n.-220+620G>A
XM_017029908.1:c.-220+620G>A	XP_016885397.1:n.-220+620G>A
XM_024452467.1:c.-220+620G>A	XP_024308235.1:n.-220+620G>A
NM_181672.3:c.751G>A MANE Select	NP_858058.1:p.Ala251Thr
NM_181673.3:c.721G>A	NP_858059.1:p.Ala241Thr