Canonical Allele Identifier: CA2821740636

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555710_71555711del , CM000685.2:g.71555710_71555711del	GRCh38
NC_000023.10:g.70775560_70775561del , CM000685.1:g.70775560_70775561del	GRCh37
NC_000023.9:g.70692285_70692286del	NCBI36
NG_015875.1:g.27649_27650del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.856-244_856-243del	ENSP00000514559.1:n.856-244_856-243del
ENST00000699750.1:c.*784-244_*784-243del	ENSP00000514560.1:n.*784-244_*784-243del
ENST00000699751.1:n.1279-970_1279-969del
ENST00000699779.1:c.*3793-244_*3793-243del	ENSP00000514585.1:n.*3793-244_*3793-243del
ENST00000699780.1:c.729-244_729-243del	ENSP00000514586.1:n.729-244_729-243del
ENST00000699781.1:c.*333-244_*333-243del	ENSP00000514587.1:n.*333-244_*333-243del
ENST00000699782.1:c.826-244_826-243del	ENSP00000514588.1:n.826-244_826-243del
ENST00000699783.1:c.895-244_895-243del	ENSP00000514589.1:n.895-244_895-243del
ENST00000699784.1:c.895-244_895-243del	ENSP00000514590.1:n.895-244_895-243del
ENST00000699785.1:c.*930-244_*930-243del	ENSP00000514591.1:n.*930-244_*930-243del
ENST00000373719.8:c.925-244_925-243del MANE Select	ENSP00000362824.3:n.925-244_925-243del
ENST00000373701.7:c.895-244_895-243del	ENSP00000362805.3:n.895-244_895-243del
ENST00000373719.7:c.925-244_925-243del	ENSP00000362824.3:n.925-244_925-243del
ENST00000459760.1:n.302-244_302-243del
ENST00000488174.5:n.4166-244_4166-243del
NM_181672.2:c.925-244_925-243del	NP_858058.1:n.925-244_925-243del
NM_181673.2:c.895-244_895-243del	NP_858059.1:n.895-244_895-243del
XM_005262308.1:c.-219-244_-219-243del	XP_005262365.1:n.-219-244_-219-243del
XM_017029908.1:c.-219-244_-219-243del	XP_016885397.1:n.-219-244_-219-243del
XM_024452467.1:c.-219-244_-219-243del	XP_024308235.1:n.-219-244_-219-243del
NM_181672.3:c.925-244_925-243del MANE Select	NP_858058.1:n.925-244_925-243del
NM_181673.3:c.895-244_895-243del	NP_858059.1:n.895-244_895-243del