Canonical Allele Identifier: CA2436503700
Gene: OGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71555168G= , CM000685.2:g.71555168G= GRCh38
NC_000023.10:g.70775018G= , CM000685.1:g.70775018G= GRCh37
NC_000023.9:g.70691743G= NCBI36
NG_015875.1:g.27107G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699749.1:c.660-22G= ENSP00000514559.1:n.660-22G=
ENST00000699750.1:c.*588-22G= ENSP00000514560.1:n.*588-22G=
ENST00000699751.1:n.1278+576G=
ENST00000699779.1:c.*3597-22G= ENSP00000514585.1:n.*3597-22G=
ENST00000699780.1:c.728+576G= ENSP00000514586.1:n.728+576G=
ENST00000699781.1:c.*332+576G= ENSP00000514587.1:n.*332+576G=
ENST00000699782.1:c.630-22G= ENSP00000514588.1:n.630-22G=
ENST00000699783.1:c.699-22G= ENSP00000514589.1:n.699-22G=
ENST00000699784.1:c.699-22G= ENSP00000514590.1:n.699-22G=
ENST00000699785.1:c.*734-22G= ENSP00000514591.1:n.*734-22G=
ENST00000373719.8:c.729-22G= MANE Select ENSP00000362824.3:n.729-22G=
ENST00000373701.7:c.699-22G= ENSP00000362805.3:n.699-22G=
ENST00000373719.7:c.729-22G= ENSP00000362824.3:n.729-22G=
ENST00000455587.3:n.608-22G=
ENST00000459760.1:n.106-22G=
ENST00000488174.5:n.4165+576G=
NM_181672.2:c.729-22G= NP_858058.1:n.729-22G=
NM_181673.2:c.699-22G= NP_858059.1:n.699-22G=
XM_005262308.1:c.-220+576G= XP_005262365.1:n.-220+576G=
XM_017029908.1:c.-220+576G= XP_016885397.1:n.-220+576G=
XM_024452467.1:c.-220+576G= XP_024308235.1:n.-220+576G=
NM_181672.3:c.729-22G= MANE Select NP_858058.1:n.729-22G=
NM_181673.3:c.699-22G= NP_858059.1:n.699-22G=