Canonical Allele Identifier: CA2821740628
Gene: OGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71555519_71555520insAGAT , CM000685.2:g.71555519_71555520insAGAT GRCh38
NC_000023.10:g.70775369_70775370insAGAT , CM000685.1:g.70775369_70775370insAGAT GRCh37
NC_000023.9:g.70692094_70692095insAGAT NCBI36
NG_015875.1:g.27458_27459insAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000699749.1:c.855+134_855+135insAGAT ENSP00000514559.1:n.855+134_855+135insAGAT
ENST00000699750.1:c.*783+134_*783+135insAGAT ENSP00000514560.1:n.*783+134_*783+135insAGAT
ENST00000699751.1:n.1278+927_1278+928insAGAT
ENST00000699779.1:c.*3792+134_*3792+135insAGAT ENSP00000514585.1:n.*3792+134_*3792+135insAGAT
ENST00000699780.1:c.729-435_729-434insAGAT ENSP00000514586.1:n.729-435_729-434insAGAT
ENST00000699781.1:c.*333-435_*333-434insAGAT ENSP00000514587.1:n.*333-435_*333-434insAGAT
ENST00000699782.1:c.825+134_825+135insAGAT ENSP00000514588.1:n.825+134_825+135insAGAT
ENST00000699783.1:c.894+134_894+135insAGAT ENSP00000514589.1:n.894+134_894+135insAGAT
ENST00000699784.1:c.894+134_894+135insAGAT ENSP00000514590.1:n.894+134_894+135insAGAT
ENST00000699785.1:c.*929+134_*929+135insAGAT ENSP00000514591.1:n.*929+134_*929+135insAGAT
ENST00000373719.8:c.924+134_924+135insAGAT MANE Select ENSP00000362824.3:n.924+134_924+135insAGAT
ENST00000373701.7:c.894+134_894+135insAGAT ENSP00000362805.3:n.894+134_894+135insAGAT
ENST00000373719.7:c.924+134_924+135insAGAT ENSP00000362824.3:n.924+134_924+135insAGAT
ENST00000459760.1:n.301+134_301+135insAGAT
ENST00000488174.5:n.4166-435_4166-434insAGAT
NM_181672.2:c.924+134_924+135insAGAT NP_858058.1:n.924+134_924+135insAGAT
NM_181673.2:c.894+134_894+135insAGAT NP_858059.1:n.894+134_894+135insAGAT
XM_005262308.1:c.-219-435_-219-434insAGAT XP_005262365.1:n.-219-435_-219-434insAGAT
XM_017029908.1:c.-219-435_-219-434insAGAT XP_016885397.1:n.-219-435_-219-434insAGAT
XM_024452467.1:c.-219-435_-219-434insAGAT XP_024308235.1:n.-219-435_-219-434insAGAT
NM_181672.3:c.924+134_924+135insAGAT MANE Select NP_858058.1:n.924+134_924+135insAGAT
NM_181673.3:c.894+134_894+135insAGAT NP_858059.1:n.894+134_894+135insAGAT