Canonical Allele Identifier: CA413545286

Gene: OGT

Linked Data

• MyVariant Identifiers: chrX:g.70775077C>T (hg19) ; chrX:g.71555227C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555227C>T , CM000685.2:g.71555227C>T	GRCh38
NC_000023.10:g.70775077C>T , CM000685.1:g.70775077C>T	GRCh37
NC_000023.9:g.70691802C>T	NCBI36
NG_015875.1:g.27166C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.697C>T	ENSP00000514559.1:p.Pro233Ser
ENST00000699750.1:c.*625C>T	ENSP00000514560.1:n.*625C>T
ENST00000699751.1:n.1278+635C>T
ENST00000699779.1:c.*3634C>T	ENSP00000514585.1:n.*3634C>T
ENST00000699780.1:c.728+635C>T	ENSP00000514586.1:n.728+635C>T
ENST00000699781.1:c.*332+635C>T	ENSP00000514587.1:n.*332+635C>T
ENST00000699782.1:c.667C>T	ENSP00000514588.1:p.Pro223Ser
ENST00000699783.1:c.736C>T	ENSP00000514589.1:p.Pro246Ser
ENST00000699784.1:c.736C>T	ENSP00000514590.1:p.Pro246Ser
ENST00000699785.1:c.*771C>T	ENSP00000514591.1:n.*771C>T
ENST00000373719.8:c.766C>T MANE Select	ENSP00000362824.3:p.Pro256Ser
ENST00000373701.7:c.736C>T	ENSP00000362805.3:p.Pro246Ser
ENST00000373719.7:c.766C>T	ENSP00000362824.3:p.Pro256Ser
ENST00000459760.1:n.143C>T
ENST00000488174.5:n.4165+635C>T
NM_181672.2:c.766C>T	NP_858058.1:p.Pro256Ser
NM_181673.2:c.736C>T	NP_858059.1:p.Pro246Ser
XM_005262308.1:c.-220+635C>T	XP_005262365.1:n.-220+635C>T
XM_017029908.1:c.-220+635C>T	XP_016885397.1:n.-220+635C>T
XM_024452467.1:c.-220+635C>T	XP_024308235.1:n.-220+635C>T
NM_181672.3:c.766C>T MANE Select	NP_858058.1:p.Pro256Ser
NM_181673.3:c.736C>T	NP_858059.1:p.Pro246Ser