Canonical Allele Identifier: CA2574401410
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240270del , CM000663.2:g.67240270del GRCh38
NC_000001.10:g.67705953del , CM000663.1:g.67705953del GRCh37
NC_000001.9:g.67478541del NCBI36
NG_011498.1:g.78785del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697148.1:c.1013del ENSP00000513137.1:n.1013del
ENST00000697149.1:c.976del ENSP00000513138.1:n.976del
ENST00000697150.1:c.1045+3468del ENSP00000513139.1:n.1045+3468del
ENST00000697151.1:c.1045+3468del ENSP00000513140.1:n.1045+3468del
ENST00000697152.1:c.799-15567del ENSP00000513141.1:n.799-15567del
ENST00000697153.1:c.795-15567del ENSP00000513142.1:n.795-15567del
ENST00000697154.1:c.956-18208del ENSP00000513143.1:n.956-18208del
ENST00000697155.1:c.649-18208del ENSP00000513144.1:n.649-18208del
ENST00000697156.1:c.1137del ENSP00000513145.1:p.Phe380SerfsTer23
ENST00000697157.1:c.991del ENSP00000513146.1:n.991del
ENST00000697158.1:c.980del ENSP00000513147.1:n.980del
ENST00000697159.1:c.830del ENSP00000513148.1:n.830del
ENST00000697160.1:c.956-15567del ENSP00000513149.1:n.956-15567del
ENST00000697161.1:c.673del ENSP00000513150.1:n.673del
ENST00000697162.1:c.1066del ENSP00000513151.1:n.1066del
ENST00000697163.1:c.1137del ENSP00000513152.1:p.Phe380SerfsTer12
ENST00000697164.1:c.1047del ENSP00000513153.1:p.Phe350SerfsTer12
ENST00000697165.1:c.834del ENSP00000513154.1:p.Phe279SerfsTer12
ENST00000697223.1:c.886del ENSP00000513190.1:n.886del
ENST00000697224.1:c.884+3468del ENSP00000513191.1:n.884+3468del
ENST00000697225.1:c.740del ENSP00000513192.1:n.740del
ENST00000697226.1:c.738+3468del ENSP00000513193.1:n.738+3468del
ENST00000697227.1:c.973del ENSP00000513194.1:n.973del
ENST00000697228.1:c.829del ENSP00000513195.1:n.829del
ENST00000697229.1:c.885-15567del ENSP00000513196.1:n.885-15567del
ENST00000697230.1:c.1047del ENSP00000513197.1:p.Phe350SerfsTer12
ENST00000697231.1:c.1042del ENSP00000513198.1:n.1042del
ENST00000697232.1:c.1066del ENSP00000513199.1:n.1066del
ENST00000347310.10:c.1137del MANE Select ENSP00000321345.5:p.Phe380SerfsTer12
ENST00000637002.1:c.528del ENSP00000490340.1:p.Phe177SerfsTer12
ENST00000347310.9:c.1137del ENSP00000321345.5:p.Phe380SerfsTer12
ENST00000395227.2:c.-58-15567del ENSP00000378652.2:n.-58-15567del
ENST00000425614.3:c.372del ENSP00000387640.2:p.Phe125SerfsTer12
ENST00000473881.2:c.191-15567del ENSP00000486667.1:n.191-15567del
NM_144701.2:c.1137del NP_653302.2:p.Phe380SerfsTer12
XM_005270516.2:c.375del XP_005270573.1:p.Phe126SerfsTer12
XM_011540789.1:c.1227del XP_011539091.1:p.Phe410SerfsTer12
XM_011540790.1:c.1137del XP_011539092.1:p.Phe380SerfsTer12
XM_011540791.1:c.1137del XP_011539093.1:p.Phe380SerfsTer12
XM_011540790.3:c.1137del XP_011539092.1:p.Phe380SerfsTer12
XM_011540791.3:c.1137del XP_011539093.1:p.Phe380SerfsTer12
XR_001736993.1:n.1228+3468del
NM_144701.3:c.1137del MANE Select NP_653302.2:p.Phe380SerfsTer12