Canonical Allele Identifier: CA2694055214

Gene: OGT

Linked Data

• gnomAD v4: X-71555685-A-ACCGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555685_71555686insCCGCT , CM000685.2:g.71555685_71555686insCCGCT	GRCh38
NC_000023.10:g.70775535_70775536insCCGCT , CM000685.1:g.70775535_70775536insCCGCT	GRCh37
NC_000023.9:g.70692260_70692261insCCGCT	NCBI36
NG_015875.1:g.27624_27625insCCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.856-269_856-268insCCGCT	ENSP00000514559.1:n.856-269_856-268insCCGCT
ENST00000699750.1:c.*784-269_*784-268insCCGCT	ENSP00000514560.1:n.*784-269_*784-268insCCGCT
ENST00000699751.1:n.1279-995_1279-994insCCGCT
ENST00000699779.1:c.*3793-269_*3793-268insCCGCT	ENSP00000514585.1:n.*3793-269_*3793-268insCCGCT
ENST00000699780.1:c.729-269_729-268insCCGCT	ENSP00000514586.1:n.729-269_729-268insCCGCT
ENST00000699781.1:c.*333-269_*333-268insCCGCT	ENSP00000514587.1:n.*333-269_*333-268insCCGCT
ENST00000699782.1:c.826-269_826-268insCCGCT	ENSP00000514588.1:n.826-269_826-268insCCGCT
ENST00000699783.1:c.895-269_895-268insCCGCT	ENSP00000514589.1:n.895-269_895-268insCCGCT
ENST00000699784.1:c.895-269_895-268insCCGCT	ENSP00000514590.1:n.895-269_895-268insCCGCT
ENST00000699785.1:c.*930-269_*930-268insCCGCT	ENSP00000514591.1:n.*930-269_*930-268insCCGCT
ENST00000373719.8:c.925-269_925-268insCCGCT MANE Select	ENSP00000362824.3:n.925-269_925-268insCCGCT
ENST00000373701.7:c.895-269_895-268insCCGCT	ENSP00000362805.3:n.895-269_895-268insCCGCT
ENST00000373719.7:c.925-269_925-268insCCGCT	ENSP00000362824.3:n.925-269_925-268insCCGCT
ENST00000459760.1:n.302-269_302-268insCCGCT
ENST00000488174.5:n.4166-269_4166-268insCCGCT
NM_181672.2:c.925-269_925-268insCCGCT	NP_858058.1:n.925-269_925-268insCCGCT
NM_181673.2:c.895-269_895-268insCCGCT	NP_858059.1:n.895-269_895-268insCCGCT
XM_005262308.1:c.-219-269_-219-268insCCGCT	XP_005262365.1:n.-219-269_-219-268insCCGCT
XM_017029908.1:c.-219-269_-219-268insCCGCT	XP_016885397.1:n.-219-269_-219-268insCCGCT
XM_024452467.1:c.-219-269_-219-268insCCGCT	XP_024308235.1:n.-219-269_-219-268insCCGCT
NM_181672.3:c.925-269_925-268insCCGCT MANE Select	NP_858058.1:n.925-269_925-268insCCGCT
NM_181673.3:c.895-269_895-268insCCGCT	NP_858059.1:n.895-269_895-268insCCGCT