Canonical Allele Identifier: CA2646125617
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240275del , CM000663.2:g.67240275del GRCh38
NC_000001.10:g.67705958del , CM000663.1:g.67705958del GRCh37
NC_000001.9:g.67478546del NCBI36
NG_011498.1:g.78790del

Transcript Alleles

HGVS Amino-acid change
ENST00000697148.1:c.1018del ENSP00000513137.1:n.1018del
ENST00000697149.1:c.981del ENSP00000513138.1:n.981del
ENST00000697150.1:c.1045+3473del ENSP00000513139.1:n.1045+3473del
ENST00000697151.1:c.1045+3473del ENSP00000513140.1:n.1045+3473del
ENST00000697152.1:c.799-15562del ENSP00000513141.1:n.799-15562del
ENST00000697153.1:c.795-15562del ENSP00000513142.1:n.795-15562del
ENST00000697154.1:c.956-18203del ENSP00000513143.1:n.956-18203del
ENST00000697155.1:c.649-18203del ENSP00000513144.1:n.649-18203del
ENST00000697156.1:c.1142del ENSP00000513145.1:p.Arg381GlnfsTer22
ENST00000697157.1:c.996del ENSP00000513146.1:n.996del
ENST00000697158.1:c.985del ENSP00000513147.1:n.985del
ENST00000697159.1:c.835del ENSP00000513148.1:n.835del
ENST00000697160.1:c.956-15562del ENSP00000513149.1:n.956-15562del
ENST00000697161.1:c.678del ENSP00000513150.1:n.678del
ENST00000697162.1:c.1071del ENSP00000513151.1:n.1071del
ENST00000697163.1:c.1142del ENSP00000513152.1:p.Arg381GlnfsTer11
ENST00000697164.1:c.1052del ENSP00000513153.1:p.Arg351GlnfsTer11
ENST00000697165.1:c.839del ENSP00000513154.1:p.Arg280GlnfsTer11
ENST00000697223.1:c.891del ENSP00000513190.1:n.891del
ENST00000697224.1:c.884+3473del ENSP00000513191.1:n.884+3473del
ENST00000697225.1:c.745del ENSP00000513192.1:n.745del
ENST00000697226.1:c.738+3473del ENSP00000513193.1:n.738+3473del
ENST00000697227.1:c.978del ENSP00000513194.1:n.978del
ENST00000697228.1:c.834del ENSP00000513195.1:n.834del
ENST00000697229.1:c.885-15562del ENSP00000513196.1:n.885-15562del
ENST00000697230.1:c.1052del ENSP00000513197.1:p.Arg351GlnfsTer11
ENST00000697231.1:c.1047del ENSP00000513198.1:n.1047del
ENST00000697232.1:c.1071del ENSP00000513199.1:n.1071del
ENST00000347310.10:c.1142del MANE Select ENSP00000321345.5:p.Arg381GlnfsTer11
ENST00000637002.1:c.533del ENSP00000490340.1:p.Arg178GlnfsTer11
ENST00000347310.9:c.1142del ENSP00000321345.5:p.Arg381GlnfsTer11
ENST00000395227.2:c.-58-15562del ENSP00000378652.2:n.-58-15562del
ENST00000425614.3:c.377del ENSP00000387640.2:p.Arg126GlnfsTer11
ENST00000473881.2:c.191-15562del ENSP00000486667.1:n.191-15562del
NM_144701.2:c.1142del NP_653302.2:p.Arg381GlnfsTer11
XM_005270516.2:c.380del XP_005270573.1:p.Arg127GlnfsTer11
XM_011540789.1:c.1232del XP_011539091.1:p.Arg411GlnfsTer11
XM_011540790.1:c.1142del XP_011539092.1:p.Arg381GlnfsTer11
XM_011540791.1:c.1142del XP_011539093.1:p.Arg381GlnfsTer11
XM_011540790.3:c.1142del XP_011539092.1:p.Arg381GlnfsTer11
XM_011540791.3:c.1142del XP_011539093.1:p.Arg381GlnfsTer11
XR_001736993.1:n.1228+3473del
NM_144701.3:c.1142del MANE Select NP_653302.2:p.Arg381GlnfsTer11