Canonical Allele Identifier: CA2436503870

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555766_71555767delinsCT , CM000685.2:g.71555766_71555767delinsCT	GRCh38
NC_000023.10:g.70775616_70775617delinsCT , CM000685.1:g.70775616_70775617delinsCT	GRCh37
NC_000023.9:g.70692341_70692342delinsCT	NCBI36
NG_015875.1:g.27705_27706delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.856-188_856-187delinsCT	ENSP00000514559.1:n.856-188_856-187delinsCT
ENST00000699750.1:c.*784-188_*784-187delinsCT	ENSP00000514560.1:n.*784-188_*784-187delinsCT
ENST00000699751.1:n.1279-914_1279-913delinsCT
ENST00000699779.1:c.*3793-188_*3793-187delinsCT	ENSP00000514585.1:n.*3793-188_*3793-187delinsCT
ENST00000699780.1:c.729-188_729-187delinsCT	ENSP00000514586.1:n.729-188_729-187delinsCT
ENST00000699781.1:c.*333-188_*333-187delinsCT	ENSP00000514587.1:n.*333-188_*333-187delinsCT
ENST00000699782.1:c.826-188_826-187delinsCT	ENSP00000514588.1:n.826-188_826-187delinsCT
ENST00000699783.1:c.895-188_895-187delinsCT	ENSP00000514589.1:n.895-188_895-187delinsCT
ENST00000699784.1:c.895-188_895-187delinsCT	ENSP00000514590.1:n.895-188_895-187delinsCT
ENST00000699785.1:c.*930-188_*930-187delinsCT	ENSP00000514591.1:n.*930-188_*930-187delinsCT
ENST00000373719.8:c.925-188_925-187delinsCT MANE Select	ENSP00000362824.3:n.925-188_925-187delinsCT
ENST00000373701.7:c.895-188_895-187delinsCT	ENSP00000362805.3:n.895-188_895-187delinsCT
ENST00000373719.7:c.925-188_925-187delinsCT	ENSP00000362824.3:n.925-188_925-187delinsCT
ENST00000459760.1:n.302-188_302-187delinsCT
ENST00000488174.5:n.4166-188_4166-187delinsCT
NM_181672.2:c.925-188_925-187delinsCT	NP_858058.1:n.925-188_925-187delinsCT
NM_181673.2:c.895-188_895-187delinsCT	NP_858059.1:n.895-188_895-187delinsCT
XM_005262308.1:c.-219-188_-219-187delinsCT	XP_005262365.1:n.-219-188_-219-187delinsCT
XM_017029908.1:c.-219-188_-219-187delinsCT	XP_016885397.1:n.-219-188_-219-187delinsCT
XM_024452467.1:c.-219-188_-219-187delinsCT	XP_024308235.1:n.-219-188_-219-187delinsCT
NM_181672.3:c.925-188_925-187delinsCT MANE Select	NP_858058.1:n.925-188_925-187delinsCT
NM_181673.3:c.895-188_895-187delinsCT	NP_858059.1:n.895-188_895-187delinsCT