Canonical Allele Identifier: CA2694055244
Gene: OGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71555720_71555721del , CM000685.2:g.71555720_71555721del GRCh38
NC_000023.10:g.70775570_70775571del , CM000685.1:g.70775570_70775571del GRCh37
NC_000023.9:g.70692295_70692296del NCBI36
NG_015875.1:g.27659_27660del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699749.1:c.856-234_856-233del ENSP00000514559.1:n.856-234_856-233del
ENST00000699750.1:c.*784-234_*784-233del ENSP00000514560.1:n.*784-234_*784-233del
ENST00000699751.1:n.1279-960_1279-959del
ENST00000699779.1:c.*3793-234_*3793-233del ENSP00000514585.1:n.*3793-234_*3793-233del
ENST00000699780.1:c.729-234_729-233del ENSP00000514586.1:n.729-234_729-233del
ENST00000699781.1:c.*333-234_*333-233del ENSP00000514587.1:n.*333-234_*333-233del
ENST00000699782.1:c.826-234_826-233del ENSP00000514588.1:n.826-234_826-233del
ENST00000699783.1:c.895-234_895-233del ENSP00000514589.1:n.895-234_895-233del
ENST00000699784.1:c.895-234_895-233del ENSP00000514590.1:n.895-234_895-233del
ENST00000699785.1:c.*930-234_*930-233del ENSP00000514591.1:n.*930-234_*930-233del
ENST00000373719.8:c.925-234_925-233del MANE Select ENSP00000362824.3:n.925-234_925-233del
ENST00000373701.7:c.895-234_895-233del ENSP00000362805.3:n.895-234_895-233del
ENST00000373719.7:c.925-234_925-233del ENSP00000362824.3:n.925-234_925-233del
ENST00000459760.1:n.302-234_302-233del
ENST00000488174.5:n.4166-234_4166-233del
NM_181672.2:c.925-234_925-233del NP_858058.1:n.925-234_925-233del
NM_181673.2:c.895-234_895-233del NP_858059.1:n.895-234_895-233del
XM_005262308.1:c.-219-234_-219-233del XP_005262365.1:n.-219-234_-219-233del
XM_017029908.1:c.-219-234_-219-233del XP_016885397.1:n.-219-234_-219-233del
XM_024452467.1:c.-219-234_-219-233del XP_024308235.1:n.-219-234_-219-233del
NM_181672.3:c.925-234_925-233del MANE Select NP_858058.1:n.925-234_925-233del
NM_181673.3:c.895-234_895-233del NP_858059.1:n.895-234_895-233del