Canonical Allele Identifier: CA413546609
Gene: OGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71555373A>C , CM000685.2:g.71555373A>C GRCh38
NC_000023.10:g.70775223A>C , CM000685.1:g.70775223A>C GRCh37
NC_000023.9:g.70691948A>C NCBI36
NG_015875.1:g.27312A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699749.1:c.843A>C ENSP00000514559.1:p.Lys281Asn
ENST00000699750.1:c.*771A>C ENSP00000514560.1:n.*771A>C
ENST00000699751.1:n.1278+781A>C
ENST00000699779.1:c.*3780A>C ENSP00000514585.1:n.*3780A>C
ENST00000699780.1:c.729-581A>C ENSP00000514586.1:n.729-581A>C
ENST00000699781.1:c.*333-581A>C ENSP00000514587.1:n.*333-581A>C
ENST00000699782.1:c.813A>C ENSP00000514588.1:p.Lys271Asn
ENST00000699783.1:c.882A>C ENSP00000514589.1:p.Lys294Asn
ENST00000699784.1:c.882A>C ENSP00000514590.1:p.Lys294Asn
ENST00000699785.1:c.*917A>C ENSP00000514591.1:n.*917A>C
ENST00000373719.8:c.912A>C MANE Select ENSP00000362824.3:p.Lys304Asn
ENST00000373701.7:c.882A>C ENSP00000362805.3:p.Lys294Asn
ENST00000373719.7:c.912A>C ENSP00000362824.3:p.Lys304Asn
ENST00000459760.1:n.289A>C
ENST00000488174.5:n.4166-581A>C
NM_181672.2:c.912A>C NP_858058.1:p.Lys304Asn
NM_181673.2:c.882A>C NP_858059.1:p.Lys294Asn
XM_005262308.1:c.-219-581A>C XP_005262365.1:n.-219-581A>C
XM_017029908.1:c.-219-581A>C XP_016885397.1:n.-219-581A>C
XM_024452467.1:c.-219-581A>C XP_024308235.1:n.-219-581A>C
NM_181672.3:c.912A>C MANE Select NP_858058.1:p.Lys304Asn
NM_181673.3:c.882A>C NP_858059.1:p.Lys294Asn