Canonical Allele Identifier: CA2743980340
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240266_67240267del , CM000663.2:g.67240266_67240267del GRCh38
NC_000001.10:g.67705949_67705950del , CM000663.1:g.67705949_67705950del GRCh37
NC_000001.9:g.67478537_67478538del NCBI36
NG_011498.1:g.78781_78782del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697148.1:c.1009_1010del ENSP00000513137.1:n.1009_1010del
ENST00000697149.1:c.972_973del ENSP00000513138.1:n.972_973del
ENST00000697150.1:c.1045+3464_1045+3465del ENSP00000513139.1:n.1045+3464_1045+3465del
ENST00000697151.1:c.1045+3464_1045+3465del ENSP00000513140.1:n.1045+3464_1045+3465del
ENST00000697152.1:c.799-15571_799-15570del ENSP00000513141.1:n.799-15571_799-15570del
ENST00000697153.1:c.795-15571_795-15570del ENSP00000513142.1:n.795-15571_795-15570del
ENST00000697154.1:c.956-18212_956-18211del ENSP00000513143.1:n.956-18212_956-18211del
ENST00000697155.1:c.649-18212_649-18211del ENSP00000513144.1:n.649-18212_649-18211del
ENST00000697156.1:c.1133_1134del ENSP00000513145.1:p.Arg378IlefsTer?
ENST00000697157.1:c.987_988del ENSP00000513146.1:n.987_988del
ENST00000697158.1:c.976_977del ENSP00000513147.1:n.976_977del
ENST00000697159.1:c.826_827del ENSP00000513148.1:n.826_827del
ENST00000697160.1:c.956-15571_956-15570del ENSP00000513149.1:n.956-15571_956-15570del
ENST00000697161.1:c.669_670del ENSP00000513150.1:n.669_670del
ENST00000697162.1:c.1062_1063del ENSP00000513151.1:n.1062_1063del
ENST00000697163.1:c.1133_1134del ENSP00000513152.1:p.Arg378IlefsTer7
ENST00000697164.1:c.1043_1044del ENSP00000513153.1:p.Arg348IlefsTer7
ENST00000697165.1:c.830_831del ENSP00000513154.1:p.Arg277IlefsTer7
ENST00000697223.1:c.882_883del ENSP00000513190.1:n.882_883del
ENST00000697224.1:c.884+3464_884+3465del ENSP00000513191.1:n.884+3464_884+3465del
ENST00000697225.1:c.736_737del ENSP00000513192.1:n.736_737del
ENST00000697226.1:c.738+3464_738+3465del ENSP00000513193.1:n.738+3464_738+3465del
ENST00000697227.1:c.969_970del ENSP00000513194.1:n.969_970del
ENST00000697228.1:c.825_826del ENSP00000513195.1:n.825_826del
ENST00000697229.1:c.885-15571_885-15570del ENSP00000513196.1:n.885-15571_885-15570del
ENST00000697230.1:c.1043_1044del ENSP00000513197.1:p.Arg348IlefsTer7
ENST00000697231.1:c.1038_1039del ENSP00000513198.1:n.1038_1039del
ENST00000697232.1:c.1062_1063del ENSP00000513199.1:n.1062_1063del
ENST00000347310.10:c.1133_1134del MANE Select ENSP00000321345.5:p.Arg378IlefsTer7
ENST00000637002.1:c.524_525del ENSP00000490340.1:p.Arg175IlefsTer7
ENST00000347310.9:c.1133_1134del ENSP00000321345.5:p.Arg378IlefsTer7
ENST00000395227.2:c.-58-15571_-58-15570del ENSP00000378652.2:n.-58-15571_-58-15570del
ENST00000425614.3:c.368_369del ENSP00000387640.2:p.Arg123IlefsTer7
ENST00000473881.2:c.191-15571_191-15570del ENSP00000486667.1:n.191-15571_191-15570del
NM_144701.2:c.1133_1134del NP_653302.2:p.Arg378IlefsTer7
XM_005270516.2:c.371_372del XP_005270573.1:p.Arg124IlefsTer7
XM_011540789.1:c.1223_1224del XP_011539091.1:p.Arg408IlefsTer7
XM_011540790.1:c.1133_1134del XP_011539092.1:p.Arg378IlefsTer7
XM_011540791.1:c.1133_1134del XP_011539093.1:p.Arg378IlefsTer7
XM_011540790.3:c.1133_1134del XP_011539092.1:p.Arg378IlefsTer7
XM_011540791.3:c.1133_1134del XP_011539093.1:p.Arg378IlefsTer7
XR_001736993.1:n.1228+3464_1228+3465del
NM_144701.3:c.1133_1134del MANE Select NP_653302.2:p.Arg378IlefsTer7