Canonical Allele Identifier: CA413545703
Gene: OGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71555273A>G , CM000685.2:g.71555273A>G GRCh38
NC_000023.10:g.70775123A>G , CM000685.1:g.70775123A>G GRCh37
NC_000023.9:g.70691848A>G NCBI36
NG_015875.1:g.27212A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699749.1:c.743A>G ENSP00000514559.1:p.Glu248Gly
ENST00000699750.1:c.*671A>G ENSP00000514560.1:n.*671A>G
ENST00000699751.1:n.1278+681A>G
ENST00000699779.1:c.*3680A>G ENSP00000514585.1:n.*3680A>G
ENST00000699780.1:c.729-681A>G ENSP00000514586.1:n.729-681A>G
ENST00000699781.1:c.*333-681A>G ENSP00000514587.1:n.*333-681A>G
ENST00000699782.1:c.713A>G ENSP00000514588.1:p.Glu238Gly
ENST00000699783.1:c.782A>G ENSP00000514589.1:p.Glu261Gly
ENST00000699784.1:c.782A>G ENSP00000514590.1:p.Glu261Gly
ENST00000699785.1:c.*817A>G ENSP00000514591.1:n.*817A>G
ENST00000373719.8:c.812A>G MANE Select ENSP00000362824.3:p.Glu271Gly
ENST00000373701.7:c.782A>G ENSP00000362805.3:p.Glu261Gly
ENST00000373719.7:c.812A>G ENSP00000362824.3:p.Glu271Gly
ENST00000459760.1:n.189A>G
ENST00000488174.5:n.4166-681A>G
NM_181672.2:c.812A>G NP_858058.1:p.Glu271Gly
NM_181673.2:c.782A>G NP_858059.1:p.Glu261Gly
XM_005262308.1:c.-219-681A>G XP_005262365.1:n.-219-681A>G
XM_017029908.1:c.-219-681A>G XP_016885397.1:n.-219-681A>G
XM_024452467.1:c.-219-681A>G XP_024308235.1:n.-219-681A>G
NM_181672.3:c.812A>G MANE Select NP_858058.1:p.Glu271Gly
NM_181673.3:c.782A>G NP_858059.1:p.Glu261Gly