Canonical Allele Identifier: CA2694055194

Gene: OGT

Linked Data

• gnomAD v4: X-71555670-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555670C>A , CM000685.2:g.71555670C>A	GRCh38
NC_000023.10:g.70775520C>A , CM000685.1:g.70775520C>A	GRCh37
NC_000023.9:g.70692245C>A	NCBI36
NG_015875.1:g.27609C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.856-284C>A	ENSP00000514559.1:n.856-284C>A
ENST00000699750.1:c.*784-284C>A	ENSP00000514560.1:n.*784-284C>A
ENST00000699751.1:n.1279-1010C>A
ENST00000699779.1:c.*3793-284C>A	ENSP00000514585.1:n.*3793-284C>A
ENST00000699780.1:c.729-284C>A	ENSP00000514586.1:n.729-284C>A
ENST00000699781.1:c.*333-284C>A	ENSP00000514587.1:n.*333-284C>A
ENST00000699782.1:c.826-284C>A	ENSP00000514588.1:n.826-284C>A
ENST00000699783.1:c.895-284C>A	ENSP00000514589.1:n.895-284C>A
ENST00000699784.1:c.895-284C>A	ENSP00000514590.1:n.895-284C>A
ENST00000699785.1:c.*930-284C>A	ENSP00000514591.1:n.*930-284C>A
ENST00000373719.8:c.925-284C>A MANE Select	ENSP00000362824.3:n.925-284C>A
ENST00000373701.7:c.895-284C>A	ENSP00000362805.3:n.895-284C>A
ENST00000373719.7:c.925-284C>A	ENSP00000362824.3:n.925-284C>A
ENST00000459760.1:n.302-284C>A
ENST00000488174.5:n.4166-284C>A
NM_181672.2:c.925-284C>A	NP_858058.1:n.925-284C>A
NM_181673.2:c.895-284C>A	NP_858059.1:n.895-284C>A
XM_005262308.1:c.-219-284C>A	XP_005262365.1:n.-219-284C>A
XM_017029908.1:c.-219-284C>A	XP_016885397.1:n.-219-284C>A
XM_024452467.1:c.-219-284C>A	XP_024308235.1:n.-219-284C>A
NM_181672.3:c.925-284C>A MANE Select	NP_858058.1:n.925-284C>A
NM_181673.3:c.895-284C>A	NP_858059.1:n.895-284C>A