Canonical Allele Identifier: CA1134103167
Gene: OGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71555711_71555712del , CM000685.2:g.71555711_71555712del GRCh38
NC_000023.10:g.70775561_70775562del , CM000685.1:g.70775561_70775562del GRCh37
NC_000023.9:g.70692286_70692287del NCBI36
NG_015875.1:g.27650_27651del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699749.1:c.856-243_856-242del ENSP00000514559.1:n.856-243_856-242del
ENST00000699750.1:c.*784-243_*784-242del ENSP00000514560.1:n.*784-243_*784-242del
ENST00000699751.1:n.1279-969_1279-968del
ENST00000699779.1:c.*3793-243_*3793-242del ENSP00000514585.1:n.*3793-243_*3793-242del
ENST00000699780.1:c.729-243_729-242del ENSP00000514586.1:n.729-243_729-242del
ENST00000699781.1:c.*333-243_*333-242del ENSP00000514587.1:n.*333-243_*333-242del
ENST00000699782.1:c.826-243_826-242del ENSP00000514588.1:n.826-243_826-242del
ENST00000699783.1:c.895-243_895-242del ENSP00000514589.1:n.895-243_895-242del
ENST00000699784.1:c.895-243_895-242del ENSP00000514590.1:n.895-243_895-242del
ENST00000699785.1:c.*930-243_*930-242del ENSP00000514591.1:n.*930-243_*930-242del
ENST00000373719.8:c.925-243_925-242del MANE Select ENSP00000362824.3:n.925-243_925-242del
ENST00000373701.7:c.895-243_895-242del ENSP00000362805.3:n.895-243_895-242del
ENST00000373719.7:c.925-243_925-242del ENSP00000362824.3:n.925-243_925-242del
ENST00000459760.1:n.302-243_302-242del
ENST00000488174.5:n.4166-243_4166-242del
NM_181672.2:c.925-243_925-242del NP_858058.1:n.925-243_925-242del
NM_181673.2:c.895-243_895-242del NP_858059.1:n.895-243_895-242del
XM_005262308.1:c.-219-243_-219-242del XP_005262365.1:n.-219-243_-219-242del
XM_017029908.1:c.-219-243_-219-242del XP_016885397.1:n.-219-243_-219-242del
XM_024452467.1:c.-219-243_-219-242del XP_024308235.1:n.-219-243_-219-242del
NM_181672.3:c.925-243_925-242del MANE Select NP_858058.1:n.925-243_925-242del
NM_181673.3:c.895-243_895-242del NP_858059.1:n.895-243_895-242del