Canonical Allele Identifier: CA2694055201

Gene: OGT

Linked Data

• gnomAD v4: X-71555676-TTGTGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555677_71555681del , CM000685.2:g.71555677_71555681del	GRCh38
NC_000023.10:g.70775527_70775531del , CM000685.1:g.70775527_70775531del	GRCh37
NC_000023.9:g.70692252_70692256del	NCBI36
NG_015875.1:g.27616_27620del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.856-277_856-273del	ENSP00000514559.1:n.856-277_856-273del
ENST00000699750.1:c.*784-277_*784-273del	ENSP00000514560.1:n.*784-277_*784-273del
ENST00000699751.1:n.1279-1003_1279-999del
ENST00000699779.1:c.*3793-277_*3793-273del	ENSP00000514585.1:n.*3793-277_*3793-273del
ENST00000699780.1:c.729-277_729-273del	ENSP00000514586.1:n.729-277_729-273del
ENST00000699781.1:c.*333-277_*333-273del	ENSP00000514587.1:n.*333-277_*333-273del
ENST00000699782.1:c.826-277_826-273del	ENSP00000514588.1:n.826-277_826-273del
ENST00000699783.1:c.895-277_895-273del	ENSP00000514589.1:n.895-277_895-273del
ENST00000699784.1:c.895-277_895-273del	ENSP00000514590.1:n.895-277_895-273del
ENST00000699785.1:c.*930-277_*930-273del	ENSP00000514591.1:n.*930-277_*930-273del
ENST00000373719.8:c.925-277_925-273del MANE Select	ENSP00000362824.3:n.925-277_925-273del
ENST00000373701.7:c.895-277_895-273del	ENSP00000362805.3:n.895-277_895-273del
ENST00000373719.7:c.925-277_925-273del	ENSP00000362824.3:n.925-277_925-273del
ENST00000459760.1:n.302-277_302-273del
ENST00000488174.5:n.4166-277_4166-273del
NM_181672.2:c.925-277_925-273del	NP_858058.1:n.925-277_925-273del
NM_181673.2:c.895-277_895-273del	NP_858059.1:n.895-277_895-273del
XM_005262308.1:c.-219-277_-219-273del	XP_005262365.1:n.-219-277_-219-273del
XM_017029908.1:c.-219-277_-219-273del	XP_016885397.1:n.-219-277_-219-273del
XM_024452467.1:c.-219-277_-219-273del	XP_024308235.1:n.-219-277_-219-273del
NM_181672.3:c.925-277_925-273del MANE Select	NP_858058.1:n.925-277_925-273del
NM_181673.3:c.895-277_895-273del	NP_858059.1:n.895-277_895-273del