Canonical Allele Identifier: CA516728064

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775115A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555265A>T , CM000685.2:g.71555265A>T	GRCh38
NC_000023.10:g.70775115A>T , CM000685.1:g.70775115A>T	GRCh37
NC_000023.9:g.70691840A>T	NCBI36
NG_015875.1:g.27204A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.735A>T	ENSP00000514559.1:p.Val245=
ENST00000699750.1:c.*663A>T	ENSP00000514560.1:n.*663A>T
ENST00000699751.1:n.1278+673A>T
ENST00000699779.1:c.*3672A>T	ENSP00000514585.1:n.*3672A>T
ENST00000699780.1:c.728+673A>T	ENSP00000514586.1:n.728+673A>T
ENST00000699781.1:c.*332+673A>T	ENSP00000514587.1:n.*332+673A>T
ENST00000699782.1:c.705A>T	ENSP00000514588.1:p.Val235=
ENST00000699783.1:c.774A>T	ENSP00000514589.1:p.Val258=
ENST00000699784.1:c.774A>T	ENSP00000514590.1:p.Val258=
ENST00000699785.1:c.*809A>T	ENSP00000514591.1:n.*809A>T
ENST00000373719.8:c.804A>T MANE Select	ENSP00000362824.3:p.Val268=
ENST00000373701.7:c.774A>T	ENSP00000362805.3:p.Val258=
ENST00000373719.7:c.804A>T	ENSP00000362824.3:p.Val268=
ENST00000459760.1:n.181A>T
ENST00000488174.5:n.4165+673A>T
NM_181672.2:c.804A>T	NP_858058.1:p.Val268=
NM_181673.2:c.774A>T	NP_858059.1:p.Val258=
XM_005262308.1:c.-220+673A>T	XP_005262365.1:n.-220+673A>T
XM_017029908.1:c.-220+673A>T	XP_016885397.1:n.-220+673A>T
XM_024452467.1:c.-220+673A>T	XP_024308235.1:n.-220+673A>T
NM_181672.3:c.804A>T MANE Select	NP_858058.1:p.Val268=
NM_181673.3:c.774A>T	NP_858059.1:p.Val258=