Canonical Allele Identifier: CA2694055078
Gene: OGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71555160_71555161insCGTG , CM000685.2:g.71555160_71555161insCGTG GRCh38
NC_000023.10:g.70775010_70775011insCGTG , CM000685.1:g.70775010_70775011insCGTG GRCh37
NC_000023.9:g.70691735_70691736insCGTG NCBI36
NG_015875.1:g.27099_27100insCGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000699749.1:c.660-30_660-29insCGTG ENSP00000514559.1:n.660-30_660-29insCGTG
ENST00000699750.1:c.*588-30_*588-29insCGTG ENSP00000514560.1:n.*588-30_*588-29insCGTG
ENST00000699751.1:n.1278+568_1278+569insCGTG
ENST00000699779.1:c.*3597-30_*3597-29insCGTG ENSP00000514585.1:n.*3597-30_*3597-29insCGTG
ENST00000699780.1:c.728+568_728+569insCGTG ENSP00000514586.1:n.728+568_728+569insCGTG
ENST00000699781.1:c.*332+568_*332+569insCGTG ENSP00000514587.1:n.*332+568_*332+569insCGTG
ENST00000699782.1:c.630-30_630-29insCGTG ENSP00000514588.1:n.630-30_630-29insCGTG
ENST00000699783.1:c.699-30_699-29insCGTG ENSP00000514589.1:n.699-30_699-29insCGTG
ENST00000699784.1:c.699-30_699-29insCGTG ENSP00000514590.1:n.699-30_699-29insCGTG
ENST00000699785.1:c.*734-30_*734-29insCGTG ENSP00000514591.1:n.*734-30_*734-29insCGTG
ENST00000373719.8:c.729-30_729-29insCGTG MANE Select ENSP00000362824.3:n.729-30_729-29insCGTG
ENST00000373701.7:c.699-30_699-29insCGTG ENSP00000362805.3:n.699-30_699-29insCGTG
ENST00000373719.7:c.729-30_729-29insCGTG ENSP00000362824.3:n.729-30_729-29insCGTG
ENST00000455587.3:n.608-30_608-29insCGTG
ENST00000459760.1:n.106-30_106-29insCGTG
ENST00000488174.5:n.4165+568_4165+569insCGTG
NM_181672.2:c.729-30_729-29insCGTG NP_858058.1:n.729-30_729-29insCGTG
NM_181673.2:c.699-30_699-29insCGTG NP_858059.1:n.699-30_699-29insCGTG
XM_005262308.1:c.-220+568_-220+569insCGTG XP_005262365.1:n.-220+568_-220+569insCGTG
XM_017029908.1:c.-220+568_-220+569insCGTG XP_016885397.1:n.-220+568_-220+569insCGTG
XM_024452467.1:c.-220+568_-220+569insCGTG XP_024308235.1:n.-220+568_-220+569insCGTG
NM_181672.3:c.729-30_729-29insCGTG MANE Select NP_858058.1:n.729-30_729-29insCGTG
NM_181673.3:c.699-30_699-29insCGTG NP_858059.1:n.699-30_699-29insCGTG