Canonical Allele Identifier: CA877838822

Gene: OGT

Linked Data

• dbSNP Id: rs1327557565
• gnomAD v3: X-71555453-G-GGCT
• gnomAD v4: X-71555453-G-GGCT
• MyVariant Identifiers: chrX:g.70775303_70775304insGCT (hg19) ; chrX:g.71555453_71555454insGCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555454_71555456dup , CM000685.2:g.71555454_71555456dup	GRCh38
NC_000023.10:g.70775304_70775306dup , CM000685.1:g.70775304_70775306dup	GRCh37
NC_000023.9:g.70692029_70692031dup	NCBI36
NG_015875.1:g.27393_27395dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.855+69_855+71dup	ENSP00000514559.1:n.855+69_855+71dup
ENST00000699750.1:c.*783+69_*783+71dup	ENSP00000514560.1:n.*783+69_*783+71dup
ENST00000699751.1:n.1278+862_1278+864dup
ENST00000699779.1:c.*3792+69_*3792+71dup	ENSP00000514585.1:n.*3792+69_*3792+71dup
ENST00000699780.1:c.729-500_729-498dup	ENSP00000514586.1:n.729-500_729-498dup
ENST00000699781.1:c.*333-500_*333-498dup	ENSP00000514587.1:n.*333-500_*333-498dup
ENST00000699782.1:c.825+69_825+71dup	ENSP00000514588.1:n.825+69_825+71dup
ENST00000699783.1:c.894+69_894+71dup	ENSP00000514589.1:n.894+69_894+71dup
ENST00000699784.1:c.894+69_894+71dup	ENSP00000514590.1:n.894+69_894+71dup
ENST00000699785.1:c.*929+69_*929+71dup	ENSP00000514591.1:n.*929+69_*929+71dup
ENST00000373719.8:c.924+69_924+71dup MANE Select	ENSP00000362824.3:n.924+69_924+71dup
ENST00000373701.7:c.894+69_894+71dup	ENSP00000362805.3:n.894+69_894+71dup
ENST00000373719.7:c.924+69_924+71dup	ENSP00000362824.3:n.924+69_924+71dup
ENST00000459760.1:n.301+69_301+71dup
ENST00000488174.5:n.4166-500_4166-498dup
NM_181672.2:c.924+69_924+71dup	NP_858058.1:n.924+69_924+71dup
NM_181673.2:c.894+69_894+71dup	NP_858059.1:n.894+69_894+71dup
XM_005262308.1:c.-219-500_-219-498dup	XP_005262365.1:n.-219-500_-219-498dup
XM_017029908.1:c.-219-500_-219-498dup	XP_016885397.1:n.-219-500_-219-498dup
XM_024452467.1:c.-219-500_-219-498dup	XP_024308235.1:n.-219-500_-219-498dup
NM_181672.3:c.924+69_924+71dup MANE Select	NP_858058.1:n.924+69_924+71dup
NM_181673.3:c.894+69_894+71dup	NP_858059.1:n.894+69_894+71dup