Canonical Allele Identifier: CA413536303

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71537917G>A , CM000685.2:g.71537917G>A	GRCh38
NC_000023.10:g.70757767G>A , CM000685.1:g.70757767G>A	GRCh37
NC_000023.9:g.70674492G>A	NCBI36
NG_015875.1:g.9856G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181672.3:c.307G>A MANE Select	NP_858058.1:p.Gly103Arg
ENST00000373719.8:c.307G>A MANE Select	ENSP00000362824.3:p.Gly103Arg
NM_181672.2:c.307G>A	NP_858058.1:p.Gly103Arg
NM_181673.2:c.277G>A	NP_858059.1:p.Gly93Arg
NM_181673.3:c.277G>A	NP_858059.1:p.Gly93Arg
ENST00000373701.7:c.277G>A	ENSP00000362805.3:p.Gly93Arg
ENST00000373719.7:c.307G>A	ENSP00000362824.3:p.Gly103Arg
ENST00000444774.3:c.256G>A	ENSP00000399729.1:p.Gly86Arg
ENST00000455587.3:n.186G>A
ENST00000488174.5:n.473G>A
ENST00000498566.3:n.307G>A
ENST00000699749.1:c.307G>A	ENSP00000514559.1:p.Gly103Arg
ENST00000699750.1:c.277G>A	ENSP00000514560.1:p.Gly93Arg
ENST00000699779.1:c.126G>A	ENSP00000514585.1:p.Glu42=
ENST00000699780.1:c.307G>A	ENSP00000514586.1:p.Gly103Arg
ENST00000699781.1:c.307G>A	ENSP00000514587.1:p.Gly103Arg
ENST00000699782.1:c.277G>A	ENSP00000514588.1:p.Gly93Arg
ENST00000699783.1:c.277G>A	ENSP00000514589.1:p.Gly93Arg
ENST00000699784.1:c.277G>A	ENSP00000514590.1:p.Gly93Arg
ENST00000699785.1:c.307G>A	ENSP00000514591.1:p.Gly103Arg
XM_017029908.1:c.-3912G>A	XP_016885397.1:n.-3912G>A
XM_024452467.1:c.-641G>A	XP_024308235.1:n.-641G>A