Canonical Allele Identifier: CA413545779

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775129G>T (hg19) ; chrX:g.71555279G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555279G>T , CM000685.2:g.71555279G>T	GRCh38
NC_000023.10:g.70775129G>T , CM000685.1:g.70775129G>T	GRCh37
NC_000023.9:g.70691854G>T	NCBI36
NG_015875.1:g.27218G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.749G>T	ENSP00000514559.1:p.Gly250Val
ENST00000699750.1:c.*677G>T	ENSP00000514560.1:n.*677G>T
ENST00000699751.1:n.1278+687G>T
ENST00000699779.1:c.*3686G>T	ENSP00000514585.1:n.*3686G>T
ENST00000699780.1:c.729-675G>T	ENSP00000514586.1:n.729-675G>T
ENST00000699781.1:c.*333-675G>T	ENSP00000514587.1:n.*333-675G>T
ENST00000699782.1:c.719G>T	ENSP00000514588.1:p.Gly240Val
ENST00000699783.1:c.788G>T	ENSP00000514589.1:p.Gly263Val
ENST00000699784.1:c.788G>T	ENSP00000514590.1:p.Gly263Val
ENST00000699785.1:c.*823G>T	ENSP00000514591.1:n.*823G>T
ENST00000373719.8:c.818G>T MANE Select	ENSP00000362824.3:p.Gly273Val
ENST00000373701.7:c.788G>T	ENSP00000362805.3:p.Gly263Val
ENST00000373719.7:c.818G>T	ENSP00000362824.3:p.Gly273Val
ENST00000459760.1:n.195G>T
ENST00000488174.5:n.4166-675G>T
NM_181672.2:c.818G>T	NP_858058.1:p.Gly273Val
NM_181673.2:c.788G>T	NP_858059.1:p.Gly263Val
XM_005262308.1:c.-219-675G>T	XP_005262365.1:n.-219-675G>T
XM_017029908.1:c.-219-675G>T	XP_016885397.1:n.-219-675G>T
XM_024452467.1:c.-219-675G>T	XP_024308235.1:n.-219-675G>T
NM_181672.3:c.818G>T MANE Select	NP_858058.1:p.Gly273Val
NM_181673.3:c.788G>T	NP_858059.1:p.Gly263Val