Canonical Allele Identifier: CA2436503809

Gene: OGT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555614_71555615delinsTG , CM000685.2:g.71555614_71555615delinsTG	GRCh38
NC_000023.10:g.70775464_70775465delinsTG , CM000685.1:g.70775464_70775465delinsTG	GRCh37
NC_000023.9:g.70692189_70692190delinsTG	NCBI36
NG_015875.1:g.27553_27554delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.855+229_855+230delinsTG	ENSP00000514559.1:n.855+229_855+230delinsTG
ENST00000699750.1:c.*783+229_*783+230delinsTG	ENSP00000514560.1:n.*783+229_*783+230delinsTG
ENST00000699751.1:n.1278+1022_1278+1023delinsTG
ENST00000699779.1:c.*3792+229_*3792+230delinsTG	ENSP00000514585.1:n.*3792+229_*3792+230delinsTG
ENST00000699780.1:c.729-340_729-339delinsTG	ENSP00000514586.1:n.729-340_729-339delinsTG
ENST00000699781.1:c.*333-340_*333-339delinsTG	ENSP00000514587.1:n.*333-340_*333-339delinsTG
ENST00000699782.1:c.825+229_825+230delinsTG	ENSP00000514588.1:n.825+229_825+230delinsTG
ENST00000699783.1:c.894+229_894+230delinsTG	ENSP00000514589.1:n.894+229_894+230delinsTG
ENST00000699784.1:c.894+229_894+230delinsTG	ENSP00000514590.1:n.894+229_894+230delinsTG
ENST00000699785.1:c.*929+229_*929+230delinsTG	ENSP00000514591.1:n.*929+229_*929+230delinsTG
ENST00000373719.8:c.924+229_924+230delinsTG MANE Select	ENSP00000362824.3:n.924+229_924+230delinsTG
ENST00000373701.7:c.894+229_894+230delinsTG	ENSP00000362805.3:n.894+229_894+230delinsTG
ENST00000373719.7:c.924+229_924+230delinsTG	ENSP00000362824.3:n.924+229_924+230delinsTG
ENST00000459760.1:n.301+229_301+230delinsTG
ENST00000488174.5:n.4166-340_4166-339delinsTG
NM_181672.2:c.924+229_924+230delinsTG	NP_858058.1:n.924+229_924+230delinsTG
NM_181673.2:c.894+229_894+230delinsTG	NP_858059.1:n.894+229_894+230delinsTG
XM_005262308.1:c.-219-340_-219-339delinsTG	XP_005262365.1:n.-219-340_-219-339delinsTG
XM_017029908.1:c.-219-340_-219-339delinsTG	XP_016885397.1:n.-219-340_-219-339delinsTG
XM_024452467.1:c.-219-340_-219-339delinsTG	XP_024308235.1:n.-219-340_-219-339delinsTG
NM_181672.3:c.924+229_924+230delinsTG MANE Select	NP_858058.1:n.924+229_924+230delinsTG
NM_181673.3:c.894+229_894+230delinsTG	NP_858059.1:n.894+229_894+230delinsTG