Canonical Allele Identifier: CA2694055253

Gene: OGT

Linked Data

• gnomAD v4: X-71555724-CAAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555728_71555731del , CM000685.2:g.71555728_71555731del	GRCh38
NC_000023.10:g.70775578_70775581del , CM000685.1:g.70775578_70775581del	GRCh37
NC_000023.9:g.70692303_70692306del	NCBI36
NG_015875.1:g.27667_27670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.856-226_856-223del	ENSP00000514559.1:n.856-226_856-223del
ENST00000699750.1:c.*784-226_*784-223del	ENSP00000514560.1:n.*784-226_*784-223del
ENST00000699751.1:n.1279-952_1279-949del
ENST00000699779.1:c.*3793-226_*3793-223del	ENSP00000514585.1:n.*3793-226_*3793-223del
ENST00000699780.1:c.729-226_729-223del	ENSP00000514586.1:n.729-226_729-223del
ENST00000699781.1:c.*333-226_*333-223del	ENSP00000514587.1:n.*333-226_*333-223del
ENST00000699782.1:c.826-226_826-223del	ENSP00000514588.1:n.826-226_826-223del
ENST00000699783.1:c.895-226_895-223del	ENSP00000514589.1:n.895-226_895-223del
ENST00000699784.1:c.895-226_895-223del	ENSP00000514590.1:n.895-226_895-223del
ENST00000699785.1:c.*930-226_*930-223del	ENSP00000514591.1:n.*930-226_*930-223del
ENST00000373719.8:c.925-226_925-223del MANE Select	ENSP00000362824.3:n.925-226_925-223del
ENST00000373701.7:c.895-226_895-223del	ENSP00000362805.3:n.895-226_895-223del
ENST00000373719.7:c.925-226_925-223del	ENSP00000362824.3:n.925-226_925-223del
ENST00000459760.1:n.302-226_302-223del
ENST00000488174.5:n.4166-226_4166-223del
NM_181672.2:c.925-226_925-223del	NP_858058.1:n.925-226_925-223del
NM_181673.2:c.895-226_895-223del	NP_858059.1:n.895-226_895-223del
XM_005262308.1:c.-219-226_-219-223del	XP_005262365.1:n.-219-226_-219-223del
XM_017029908.1:c.-219-226_-219-223del	XP_016885397.1:n.-219-226_-219-223del
XM_024452467.1:c.-219-226_-219-223del	XP_024308235.1:n.-219-226_-219-223del
NM_181672.3:c.925-226_925-223del MANE Select	NP_858058.1:n.925-226_925-223del
NM_181673.3:c.895-226_895-223del	NP_858059.1:n.895-226_895-223del