Canonical Allele Identifier: CA2579717568

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555288_71555296del , CM000685.2:g.71555288_71555296del	GRCh38
NC_000023.10:g.70775138_70775146del , CM000685.1:g.70775138_70775146del	GRCh37
NC_000023.9:g.70691863_70691871del	NCBI36
NG_015875.1:g.27227_27235del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.758_766del	ENSP00000514559.1:p.Asp253_Ile256delinsVal
ENST00000699750.1:c.*686_*694del	ENSP00000514560.1:n.*686_*694del
ENST00000699751.1:n.1278+696_1278+704del
ENST00000699779.1:c.*3695_*3703del	ENSP00000514585.1:n.*3695_*3703del
ENST00000699780.1:c.729-666_729-658del	ENSP00000514586.1:n.729-666_729-658del
ENST00000699781.1:c.*333-666_*333-658del	ENSP00000514587.1:n.*333-666_*333-658del
ENST00000699782.1:c.728_736del	ENSP00000514588.1:p.Asp243_Ile246delinsVal
ENST00000699783.1:c.797_805del	ENSP00000514589.1:p.Asp266_Ile269delinsVal
ENST00000699784.1:c.797_805del	ENSP00000514590.1:p.Asp266_Ile269delinsVal
ENST00000699785.1:c.*832_*840del	ENSP00000514591.1:n.*832_*840del
ENST00000373719.8:c.827_835del MANE Select	ENSP00000362824.3:p.Asp276_Ile279delinsVal
ENST00000373701.7:c.797_805del	ENSP00000362805.3:p.Asp266_Ile269delinsVal
ENST00000373719.7:c.827_835del	ENSP00000362824.3:p.Asp276_Ile279delinsVal
ENST00000459760.1:n.204_212del
ENST00000488174.5:n.4166-666_4166-658del
NM_181672.2:c.827_835del	NP_858058.1:p.Asp276_Ile279delinsVal
NM_181673.2:c.797_805del	NP_858059.1:p.Asp266_Ile269delinsVal
XM_005262308.1:c.-219-666_-219-658del	XP_005262365.1:n.-219-666_-219-658del
XM_017029908.1:c.-219-666_-219-658del	XP_016885397.1:n.-219-666_-219-658del
XM_024452467.1:c.-219-666_-219-658del	XP_024308235.1:n.-219-666_-219-658del
NM_181672.3:c.827_835del MANE Select	NP_858058.1:p.Asp276_Ile279delinsVal
NM_181673.3:c.797_805del	NP_858059.1:p.Asp266_Ile269delinsVal