Canonical Allele Identifier: CA2436503857

Gene: OGT

Linked Data

• dbSNP Id: rs2040338583
• gnomAD v4: X-71555740-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71555740A>C , CM000685.2:g.71555740A>C	GRCh38
NC_000023.10:g.70775590A>C , CM000685.1:g.70775590A>C	GRCh37
NC_000023.9:g.70692315A>C	NCBI36
NG_015875.1:g.27679A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699749.1:c.856-214A>C	ENSP00000514559.1:n.856-214A>C
ENST00000699750.1:c.*784-214A>C	ENSP00000514560.1:n.*784-214A>C
ENST00000699751.1:n.1279-940A>C
ENST00000699779.1:c.*3793-214A>C	ENSP00000514585.1:n.*3793-214A>C
ENST00000699780.1:c.729-214A>C	ENSP00000514586.1:n.729-214A>C
ENST00000699781.1:c.*333-214A>C	ENSP00000514587.1:n.*333-214A>C
ENST00000699782.1:c.826-214A>C	ENSP00000514588.1:n.826-214A>C
ENST00000699783.1:c.895-214A>C	ENSP00000514589.1:n.895-214A>C
ENST00000699784.1:c.895-214A>C	ENSP00000514590.1:n.895-214A>C
ENST00000699785.1:c.*930-214A>C	ENSP00000514591.1:n.*930-214A>C
ENST00000373719.8:c.925-214A>C MANE Select	ENSP00000362824.3:n.925-214A>C
ENST00000373701.7:c.895-214A>C	ENSP00000362805.3:n.895-214A>C
ENST00000373719.7:c.925-214A>C	ENSP00000362824.3:n.925-214A>C
ENST00000459760.1:n.302-214A>C
ENST00000488174.5:n.4166-214A>C
NM_181672.2:c.925-214A>C	NP_858058.1:n.925-214A>C
NM_181673.2:c.895-214A>C	NP_858059.1:n.895-214A>C
XM_005262308.1:c.-219-214A>C	XP_005262365.1:n.-219-214A>C
XM_017029908.1:c.-219-214A>C	XP_016885397.1:n.-219-214A>C
XM_024452467.1:c.-219-214A>C	XP_024308235.1:n.-219-214A>C
NM_181672.3:c.925-214A>C MANE Select	NP_858058.1:n.925-214A>C
NM_181673.3:c.895-214A>C	NP_858059.1:n.895-214A>C