Canonical Allele Identifier: CA2694055133

Gene: OGT

Linked Data

• gnomAD v4: X-71555447-TGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555452_71555454del , CM000685.2:g.71555452_71555454del	GRCh38
NC_000023.10:g.70775302_70775304del , CM000685.1:g.70775302_70775304del	GRCh37
NC_000023.9:g.70692027_70692029del	NCBI36
NG_015875.1:g.27391_27393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.855+67_855+69del	ENSP00000514559.1:n.855+67_855+69del
ENST00000699750.1:c.*783+67_*783+69del	ENSP00000514560.1:n.*783+67_*783+69del
ENST00000699751.1:n.1278+860_1278+862del
ENST00000699779.1:c.*3792+67_*3792+69del	ENSP00000514585.1:n.*3792+67_*3792+69del
ENST00000699780.1:c.729-502_729-500del	ENSP00000514586.1:n.729-502_729-500del
ENST00000699781.1:c.*333-502_*333-500del	ENSP00000514587.1:n.*333-502_*333-500del
ENST00000699782.1:c.825+67_825+69del	ENSP00000514588.1:n.825+67_825+69del
ENST00000699783.1:c.894+67_894+69del	ENSP00000514589.1:n.894+67_894+69del
ENST00000699784.1:c.894+67_894+69del	ENSP00000514590.1:n.894+67_894+69del
ENST00000699785.1:c.*929+67_*929+69del	ENSP00000514591.1:n.*929+67_*929+69del
ENST00000373719.8:c.924+67_924+69del MANE Select	ENSP00000362824.3:n.924+67_924+69del
ENST00000373701.7:c.894+67_894+69del	ENSP00000362805.3:n.894+67_894+69del
ENST00000373719.7:c.924+67_924+69del	ENSP00000362824.3:n.924+67_924+69del
ENST00000459760.1:n.301+67_301+69del
ENST00000488174.5:n.4166-502_4166-500del
NM_181672.2:c.924+67_924+69del	NP_858058.1:n.924+67_924+69del
NM_181673.2:c.894+67_894+69del	NP_858059.1:n.894+67_894+69del
XM_005262308.1:c.-219-502_-219-500del	XP_005262365.1:n.-219-502_-219-500del
XM_017029908.1:c.-219-502_-219-500del	XP_016885397.1:n.-219-502_-219-500del
XM_024452467.1:c.-219-502_-219-500del	XP_024308235.1:n.-219-502_-219-500del
NM_181672.3:c.924+67_924+69del MANE Select	NP_858058.1:n.924+67_924+69del
NM_181673.3:c.894+67_894+69del	NP_858059.1:n.894+67_894+69del