Canonical Allele Identifier: CA516728097

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775133G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555283G>T , CM000685.2:g.71555283G>T	GRCh38
NC_000023.10:g.70775133G>T , CM000685.1:g.70775133G>T	GRCh37
NC_000023.9:g.70691858G>T	NCBI36
NG_015875.1:g.27222G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.753G>T	ENSP00000514559.1:p.Leu251=
ENST00000699750.1:c.*681G>T	ENSP00000514560.1:n.*681G>T
ENST00000699751.1:n.1278+691G>T
ENST00000699779.1:c.*3690G>T	ENSP00000514585.1:n.*3690G>T
ENST00000699780.1:c.729-671G>T	ENSP00000514586.1:n.729-671G>T
ENST00000699781.1:c.*333-671G>T	ENSP00000514587.1:n.*333-671G>T
ENST00000699782.1:c.723G>T	ENSP00000514588.1:p.Leu241=
ENST00000699783.1:c.792G>T	ENSP00000514589.1:p.Leu264=
ENST00000699784.1:c.792G>T	ENSP00000514590.1:p.Leu264=
ENST00000699785.1:c.*827G>T	ENSP00000514591.1:n.*827G>T
ENST00000373719.8:c.822G>T MANE Select	ENSP00000362824.3:p.Leu274=
ENST00000373701.7:c.792G>T	ENSP00000362805.3:p.Leu264=
ENST00000373719.7:c.822G>T	ENSP00000362824.3:p.Leu274=
ENST00000459760.1:n.199G>T
ENST00000488174.5:n.4166-671G>T
NM_181672.2:c.822G>T	NP_858058.1:p.Leu274=
NM_181673.2:c.792G>T	NP_858059.1:p.Leu264=
XM_005262308.1:c.-219-671G>T	XP_005262365.1:n.-219-671G>T
XM_017029908.1:c.-219-671G>T	XP_016885397.1:n.-219-671G>T
XM_024452467.1:c.-219-671G>T	XP_024308235.1:n.-219-671G>T
NM_181672.3:c.822G>T MANE Select	NP_858058.1:p.Leu274=
NM_181673.3:c.792G>T	NP_858059.1:p.Leu264=