Canonical Allele Identifier: CA2574401411
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240282del , CM000663.2:g.67240282del GRCh38
NC_000001.10:g.67705965del , CM000663.1:g.67705965del GRCh37
NC_000001.9:g.67478553del NCBI36
NG_011498.1:g.78797del

Transcript Alleles

HGVS Amino-acid change
ENST00000697148.1:c.1024+1del
ENST00000697149.1:c.987+1del
ENST00000697150.1:c.1045+3480del ENSP00000513139.1:n.1045+3480del
ENST00000697151.1:c.1045+3480del ENSP00000513140.1:n.1045+3480del
ENST00000697152.1:c.799-15555del ENSP00000513141.1:n.799-15555del
ENST00000697153.1:c.795-15555del ENSP00000513142.1:n.795-15555del
ENST00000697154.1:c.956-18196del ENSP00000513143.1:n.956-18196del
ENST00000697155.1:c.649-18196del ENSP00000513144.1:n.649-18196del
ENST00000697156.1:c.1148+1del
ENST00000697157.1:c.1002+1del
ENST00000697158.1:c.991+1del
ENST00000697159.1:c.841+1del
ENST00000697160.1:c.956-15555del ENSP00000513149.1:n.956-15555del
ENST00000697161.1:c.684+1del
ENST00000697162.1:c.1077+1del
ENST00000697163.1:c.1148+1del
ENST00000697164.1:c.1058+1del
ENST00000697165.1:c.845+1del
ENST00000697223.1:c.897+1del
ENST00000697224.1:c.884+3480del ENSP00000513191.1:n.884+3480del
ENST00000697225.1:c.751+1del
ENST00000697226.1:c.738+3480del ENSP00000513193.1:n.738+3480del
ENST00000697227.1:c.984+1del
ENST00000697228.1:c.840+1del
ENST00000697229.1:c.885-15555del ENSP00000513196.1:n.885-15555del
ENST00000697230.1:c.1058+1del
ENST00000697231.1:c.1053+1del
ENST00000697232.1:c.1077+1del
ENST00000347310.10:c.1148+1del
ENST00000637002.1:c.539+1del
ENST00000347310.9:c.1148+1del
ENST00000395227.2:c.-58-15555del ENSP00000378652.2:n.-58-15555del
ENST00000425614.3:c.383+1del
ENST00000473881.2:c.191-15555del ENSP00000486667.1:n.191-15555del
NM_144701.2:c.1148+1del
XM_005270516.2:c.386+1del
XM_011540789.1:c.1238+1del
XM_011540790.1:c.1148+1del
XM_011540791.1:c.1148+1del
XM_011540790.3:c.1148+1del
XM_011540791.3:c.1148+1del
XR_001736993.1:n.1228+3480del
NM_144701.3:c.1148+1del