Canonical Allele Identifier: CA2694055155

Gene: OGT

Linked Data

• gnomAD v4: X-71555481-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555481G>T , CM000685.2:g.71555481G>T	GRCh38
NC_000023.10:g.70775331G>T , CM000685.1:g.70775331G>T	GRCh37
NC_000023.9:g.70692056G>T	NCBI36
NG_015875.1:g.27420G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.855+96G>T	ENSP00000514559.1:n.855+96G>T
ENST00000699750.1:c.*783+96G>T	ENSP00000514560.1:n.*783+96G>T
ENST00000699751.1:n.1278+889G>T
ENST00000699779.1:c.*3792+96G>T	ENSP00000514585.1:n.*3792+96G>T
ENST00000699780.1:c.729-473G>T	ENSP00000514586.1:n.729-473G>T
ENST00000699781.1:c.*333-473G>T	ENSP00000514587.1:n.*333-473G>T
ENST00000699782.1:c.825+96G>T	ENSP00000514588.1:n.825+96G>T
ENST00000699783.1:c.894+96G>T	ENSP00000514589.1:n.894+96G>T
ENST00000699784.1:c.894+96G>T	ENSP00000514590.1:n.894+96G>T
ENST00000699785.1:c.*929+96G>T	ENSP00000514591.1:n.*929+96G>T
ENST00000373719.8:c.924+96G>T MANE Select	ENSP00000362824.3:n.924+96G>T
ENST00000373701.7:c.894+96G>T	ENSP00000362805.3:n.894+96G>T
ENST00000373719.7:c.924+96G>T	ENSP00000362824.3:n.924+96G>T
ENST00000459760.1:n.301+96G>T
ENST00000488174.5:n.4166-473G>T
NM_181672.2:c.924+96G>T	NP_858058.1:n.924+96G>T
NM_181673.2:c.894+96G>T	NP_858059.1:n.894+96G>T
XM_005262308.1:c.-219-473G>T	XP_005262365.1:n.-219-473G>T
XM_017029908.1:c.-219-473G>T	XP_016885397.1:n.-219-473G>T
XM_024452467.1:c.-219-473G>T	XP_024308235.1:n.-219-473G>T
NM_181672.3:c.924+96G>T MANE Select	NP_858058.1:n.924+96G>T
NM_181673.3:c.894+96G>T	NP_858059.1:n.894+96G>T