Canonical Allele Identifier: CA2579717565
Gene: OGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71555178_71555181del , CM000685.2:g.71555178_71555181del GRCh38
NC_000023.10:g.70775028_70775031del , CM000685.1:g.70775028_70775031del GRCh37
NC_000023.9:g.70691753_70691756del NCBI36
NG_015875.1:g.27117_27120del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699749.1:c.660-12_660-9del ENSP00000514559.1:n.660-12_660-9del
ENST00000699750.1:c.*588-12_*588-9del ENSP00000514560.1:n.*588-12_*588-9del
ENST00000699751.1:n.1278+586_1278+589del
ENST00000699779.1:c.*3597-12_*3597-9del ENSP00000514585.1:n.*3597-12_*3597-9del
ENST00000699780.1:c.728+586_728+589del ENSP00000514586.1:n.728+586_728+589del
ENST00000699781.1:c.*332+586_*332+589del ENSP00000514587.1:n.*332+586_*332+589del
ENST00000699782.1:c.630-12_630-9del ENSP00000514588.1:n.630-12_630-9del
ENST00000699783.1:c.699-12_699-9del ENSP00000514589.1:n.699-12_699-9del
ENST00000699784.1:c.699-12_699-9del ENSP00000514590.1:n.699-12_699-9del
ENST00000699785.1:c.*734-12_*734-9del ENSP00000514591.1:n.*734-12_*734-9del
ENST00000373719.8:c.729-12_729-9del MANE Select ENSP00000362824.3:n.729-12_729-9del
ENST00000373701.7:c.699-12_699-9del ENSP00000362805.3:n.699-12_699-9del
ENST00000373719.7:c.729-12_729-9del ENSP00000362824.3:n.729-12_729-9del
ENST00000455587.3:n.608-12_608-9del
ENST00000459760.1:n.106-12_106-9del
ENST00000488174.5:n.4165+586_4165+589del
NM_181672.2:c.729-12_729-9del NP_858058.1:n.729-12_729-9del
NM_181673.2:c.699-12_699-9del NP_858059.1:n.699-12_699-9del
XM_005262308.1:c.-220+586_-220+589del XP_005262365.1:n.-220+586_-220+589del
XM_017029908.1:c.-220+586_-220+589del XP_016885397.1:n.-220+586_-220+589del
XM_024452467.1:c.-220+586_-220+589del XP_024308235.1:n.-220+586_-220+589del
NM_181672.3:c.729-12_729-9del MANE Select NP_858058.1:n.729-12_729-9del
NM_181673.3:c.699-12_699-9del NP_858059.1:n.699-12_699-9del