Canonical Allele Identifier: CA413545998

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775153C>G (hg19) ; chrX:g.71555303C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555303C>G , CM000685.2:g.71555303C>G	GRCh38
NC_000023.10:g.70775153C>G , CM000685.1:g.70775153C>G	GRCh37
NC_000023.9:g.70691878C>G	NCBI36
NG_015875.1:g.27242C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.773C>G	ENSP00000514559.1:p.Thr258Ser
ENST00000699750.1:c.*701C>G	ENSP00000514560.1:n.*701C>G
ENST00000699751.1:n.1278+711C>G
ENST00000699779.1:c.*3710C>G	ENSP00000514585.1:n.*3710C>G
ENST00000699780.1:c.729-651C>G	ENSP00000514586.1:n.729-651C>G
ENST00000699781.1:c.*333-651C>G	ENSP00000514587.1:n.*333-651C>G
ENST00000699782.1:c.743C>G	ENSP00000514588.1:p.Thr248Ser
ENST00000699783.1:c.812C>G	ENSP00000514589.1:p.Thr271Ser
ENST00000699784.1:c.812C>G	ENSP00000514590.1:p.Thr271Ser
ENST00000699785.1:c.*847C>G	ENSP00000514591.1:n.*847C>G
ENST00000373719.8:c.842C>G MANE Select	ENSP00000362824.3:p.Thr281Ser
ENST00000373701.7:c.812C>G	ENSP00000362805.3:p.Thr271Ser
ENST00000373719.7:c.842C>G	ENSP00000362824.3:p.Thr281Ser
ENST00000459760.1:n.219C>G
ENST00000488174.5:n.4166-651C>G
NM_181672.2:c.842C>G	NP_858058.1:p.Thr281Ser
NM_181673.2:c.812C>G	NP_858059.1:p.Thr271Ser
XM_005262308.1:c.-219-651C>G	XP_005262365.1:n.-219-651C>G
XM_017029908.1:c.-219-651C>G	XP_016885397.1:n.-219-651C>G
XM_024452467.1:c.-219-651C>G	XP_024308235.1:n.-219-651C>G
NM_181672.3:c.842C>G MANE Select	NP_858058.1:p.Thr281Ser
NM_181673.3:c.812C>G	NP_858059.1:p.Thr271Ser