Canonical Allele Identifier: CA2579717527

Gene: OGT

Linked Data

• gnomAD v4: X-71555135-TGTGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555136_71555140del , CM000685.2:g.71555136_71555140del	GRCh38
NC_000023.10:g.70774986_70774990del , CM000685.1:g.70774986_70774990del	GRCh37
NC_000023.9:g.70691711_70691715del	NCBI36
NG_015875.1:g.27075_27079del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.660-54_660-50del	ENSP00000514559.1:n.660-54_660-50del
ENST00000699750.1:c.*588-54_*588-50del	ENSP00000514560.1:n.*588-54_*588-50del
ENST00000699751.1:n.1278+544_1278+548del
ENST00000699779.1:c.*3597-54_*3597-50del	ENSP00000514585.1:n.*3597-54_*3597-50del
ENST00000699780.1:c.728+544_728+548del	ENSP00000514586.1:n.728+544_728+548del
ENST00000699781.1:c.*332+544_*332+548del	ENSP00000514587.1:n.*332+544_*332+548del
ENST00000699782.1:c.630-54_630-50del	ENSP00000514588.1:n.630-54_630-50del
ENST00000699783.1:c.699-54_699-50del	ENSP00000514589.1:n.699-54_699-50del
ENST00000699784.1:c.699-54_699-50del	ENSP00000514590.1:n.699-54_699-50del
ENST00000699785.1:c.*734-54_*734-50del	ENSP00000514591.1:n.*734-54_*734-50del
ENST00000373719.8:c.729-54_729-50del MANE Select	ENSP00000362824.3:n.729-54_729-50del
ENST00000373701.7:c.699-54_699-50del	ENSP00000362805.3:n.699-54_699-50del
ENST00000373719.7:c.729-54_729-50del	ENSP00000362824.3:n.729-54_729-50del
ENST00000455587.3:n.608-54_608-50del
ENST00000459760.1:n.106-54_106-50del
ENST00000488174.5:n.4165+544_4165+548del
NM_181672.2:c.729-54_729-50del	NP_858058.1:n.729-54_729-50del
NM_181673.2:c.699-54_699-50del	NP_858059.1:n.699-54_699-50del
XM_005262308.1:c.-220+544_-220+548del	XP_005262365.1:n.-220+544_-220+548del
XM_017029908.1:c.-220+544_-220+548del	XP_016885397.1:n.-220+544_-220+548del
XM_024452467.1:c.-220+544_-220+548del	XP_024308235.1:n.-220+544_-220+548del
NM_181672.3:c.729-54_729-50del MANE Select	NP_858058.1:n.729-54_729-50del
NM_181673.3:c.699-54_699-50del	NP_858059.1:n.699-54_699-50del