Canonical Allele Identifier: CA2436503730

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555296A= , CM000685.2:g.71555296A=	GRCh38
NC_000023.10:g.70775146A= , CM000685.1:g.70775146A=	GRCh37
NC_000023.9:g.70691871A=	NCBI36
NG_015875.1:g.27235A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.766A=	ENSP00000514559.1:p.Ile256=
ENST00000699750.1:c.*694A=	ENSP00000514560.1:n.*694A=
ENST00000699751.1:n.1278+704A=
ENST00000699779.1:c.*3703A=	ENSP00000514585.1:n.*3703A=
ENST00000699780.1:c.729-658A=	ENSP00000514586.1:n.729-658A=
ENST00000699781.1:c.*333-658A=	ENSP00000514587.1:n.*333-658A=
ENST00000699782.1:c.736A=	ENSP00000514588.1:p.Ile246=
ENST00000699783.1:c.805A=	ENSP00000514589.1:p.Ile269=
ENST00000699784.1:c.805A=	ENSP00000514590.1:p.Ile269=
ENST00000699785.1:c.*840A=	ENSP00000514591.1:n.*840A=
ENST00000373719.8:c.835A= MANE Select	ENSP00000362824.3:p.Ile279=
ENST00000373701.7:c.805A=	ENSP00000362805.3:p.Ile269=
ENST00000373719.7:c.835A=	ENSP00000362824.3:p.Ile279=
ENST00000459760.1:n.212A=
ENST00000488174.5:n.4166-658A=
NM_181672.2:c.835A=	NP_858058.1:p.Ile279=
NM_181673.2:c.805A=	NP_858059.1:p.Ile269=
XM_005262308.1:c.-219-658A=	XP_005262365.1:n.-219-658A=
XM_017029908.1:c.-219-658A=	XP_016885397.1:n.-219-658A=
XM_024452467.1:c.-219-658A=	XP_024308235.1:n.-219-658A=
NM_181672.3:c.835A= MANE Select	NP_858058.1:p.Ile279=
NM_181673.3:c.805A=	NP_858059.1:p.Ile269=