Canonical Allele Identifier: CA413546157

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775168T>C (hg19) ; chrX:g.71555318T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555318T>C , CM000685.2:g.71555318T>C	GRCh38
NC_000023.10:g.70775168T>C , CM000685.1:g.70775168T>C	GRCh37
NC_000023.9:g.70691893T>C	NCBI36
NG_015875.1:g.27257T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.788T>C	ENSP00000514559.1:p.Ile263Thr
ENST00000699750.1:c.*716T>C	ENSP00000514560.1:n.*716T>C
ENST00000699751.1:n.1278+726T>C
ENST00000699779.1:c.*3725T>C	ENSP00000514585.1:n.*3725T>C
ENST00000699780.1:c.729-636T>C	ENSP00000514586.1:n.729-636T>C
ENST00000699781.1:c.*333-636T>C	ENSP00000514587.1:n.*333-636T>C
ENST00000699782.1:c.758T>C	ENSP00000514588.1:p.Ile253Thr
ENST00000699783.1:c.827T>C	ENSP00000514589.1:p.Ile276Thr
ENST00000699784.1:c.827T>C	ENSP00000514590.1:p.Ile276Thr
ENST00000699785.1:c.*862T>C	ENSP00000514591.1:n.*862T>C
ENST00000373719.8:c.857T>C MANE Select	ENSP00000362824.3:p.Ile286Thr
ENST00000373701.7:c.827T>C	ENSP00000362805.3:p.Ile276Thr
ENST00000373719.7:c.857T>C	ENSP00000362824.3:p.Ile286Thr
ENST00000459760.1:n.234T>C
ENST00000488174.5:n.4166-636T>C
NM_181672.2:c.857T>C	NP_858058.1:p.Ile286Thr
NM_181673.2:c.827T>C	NP_858059.1:p.Ile276Thr
XM_005262308.1:c.-219-636T>C	XP_005262365.1:n.-219-636T>C
XM_017029908.1:c.-219-636T>C	XP_016885397.1:n.-219-636T>C
XM_024452467.1:c.-219-636T>C	XP_024308235.1:n.-219-636T>C
NM_181672.3:c.857T>C MANE Select	NP_858058.1:p.Ile286Thr
NM_181673.3:c.827T>C	NP_858059.1:p.Ile276Thr