Canonical Allele Identifier: CA413545554

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775107G>T (hg19) ; chrX:g.71555257G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555257G>T , CM000685.2:g.71555257G>T	GRCh38
NC_000023.10:g.70775107G>T , CM000685.1:g.70775107G>T	GRCh37
NC_000023.9:g.70691832G>T	NCBI36
NG_015875.1:g.27196G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.727G>T	ENSP00000514559.1:p.Ala243Ser
ENST00000699750.1:c.*655G>T	ENSP00000514560.1:n.*655G>T
ENST00000699751.1:n.1278+665G>T
ENST00000699779.1:c.*3664G>T	ENSP00000514585.1:n.*3664G>T
ENST00000699780.1:c.728+665G>T	ENSP00000514586.1:n.728+665G>T
ENST00000699781.1:c.*332+665G>T	ENSP00000514587.1:n.*332+665G>T
ENST00000699782.1:c.697G>T	ENSP00000514588.1:p.Ala233Ser
ENST00000699783.1:c.766G>T	ENSP00000514589.1:p.Ala256Ser
ENST00000699784.1:c.766G>T	ENSP00000514590.1:p.Ala256Ser
ENST00000699785.1:c.*801G>T	ENSP00000514591.1:n.*801G>T
ENST00000373719.8:c.796G>T MANE Select	ENSP00000362824.3:p.Ala266Ser
ENST00000373701.7:c.766G>T	ENSP00000362805.3:p.Ala256Ser
ENST00000373719.7:c.796G>T	ENSP00000362824.3:p.Ala266Ser
ENST00000459760.1:n.173G>T
ENST00000488174.5:n.4165+665G>T
NM_181672.2:c.796G>T	NP_858058.1:p.Ala266Ser
NM_181673.2:c.766G>T	NP_858059.1:p.Ala256Ser
XM_005262308.1:c.-220+665G>T	XP_005262365.1:n.-220+665G>T
XM_017029908.1:c.-220+665G>T	XP_016885397.1:n.-220+665G>T
XM_024452467.1:c.-220+665G>T	XP_024308235.1:n.-220+665G>T
NM_181672.3:c.796G>T MANE Select	NP_858058.1:p.Ala266Ser
NM_181673.3:c.766G>T	NP_858059.1:p.Ala256Ser