Canonical Allele Identifier: CA10447585

Gene: OGT

Linked Data

• dbSNP Id: rs771394145
• ExAC: X:70775008 GTGTGTGTGTGTGTGTGTGTGTT / G
• gnomAD v3: X-71555158-GTGTGTGTGTGTGTGTGTGTGTT-G
• gnomAD v4: X-71555158-GTGTGTGTGTGTGTGTGTGTGTT-G
• MyVariant Identifiers: chrX:g.70775009_70775030del (hg19) ; chrX:g.71555159_71555180del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555160_71555181del , CM000685.2:g.71555160_71555181del	GRCh38
NC_000023.10:g.70775010_70775031del , CM000685.1:g.70775010_70775031del	GRCh37
NC_000023.9:g.70691735_70691756del	NCBI36
NG_015875.1:g.27099_27120del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-30_660-9del	ENSP00000514559.1:n.660-30_660-9del
ENST00000699750.1:c.*588-30_*588-9del	ENSP00000514560.1:n.*588-30_*588-9del
ENST00000699751.1:n.1278+568_1278+589del
ENST00000699779.1:c.*3597-30_*3597-9del	ENSP00000514585.1:n.*3597-30_*3597-9del
ENST00000699780.1:c.728+568_728+589del	ENSP00000514586.1:n.728+568_728+589del
ENST00000699781.1:c.*332+568_*332+589del	ENSP00000514587.1:n.*332+568_*332+589del
ENST00000699782.1:c.630-30_630-9del	ENSP00000514588.1:n.630-30_630-9del
ENST00000699783.1:c.699-30_699-9del	ENSP00000514589.1:n.699-30_699-9del
ENST00000699784.1:c.699-30_699-9del	ENSP00000514590.1:n.699-30_699-9del
ENST00000699785.1:c.*734-30_*734-9del	ENSP00000514591.1:n.*734-30_*734-9del
ENST00000373719.8:c.729-30_729-9del MANE Select	ENSP00000362824.3:n.729-30_729-9del
ENST00000373701.7:c.699-30_699-9del	ENSP00000362805.3:n.699-30_699-9del
ENST00000373719.7:c.729-30_729-9del	ENSP00000362824.3:n.729-30_729-9del
ENST00000455587.3:n.608-30_608-9del
ENST00000459760.1:n.106-30_106-9del
ENST00000488174.5:n.4165+568_4165+589del
NM_181672.2:c.729-30_729-9del	NP_858058.1:n.729-30_729-9del
NM_181673.2:c.699-30_699-9del	NP_858059.1:n.699-30_699-9del
XM_005262308.1:c.-220+568_-220+589del	XP_005262365.1:n.-220+568_-220+589del
XM_017029908.1:c.-220+568_-220+589del	XP_016885397.1:n.-220+568_-220+589del
XM_024452467.1:c.-220+568_-220+589del	XP_024308235.1:n.-220+568_-220+589del
NM_181672.3:c.729-30_729-9del MANE Select	NP_858058.1:n.729-30_729-9del
NM_181673.3:c.699-30_699-9del	NP_858059.1:n.699-30_699-9del