Canonical Allele Identifier: CA2574401381
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67236834_67236844del , CM000663.2:g.67236834_67236844del GRCh38
NC_000001.10:g.67702517_67702527del , CM000663.1:g.67702517_67702527del GRCh37
NC_000001.9:g.67475105_67475115del NCBI36
NG_011498.1:g.75349_75359del

Transcript Alleles

HGVS Amino-acid change
ENST00000697148.1:c.921+32_921+42del ENSP00000513137.1:n.921+32_921+42del
ENST00000697149.1:c.884+32_884+42del ENSP00000513138.1:n.884+32_884+42del
ENST00000697150.1:c.1045+32_1045+42del ENSP00000513139.1:n.1045+32_1045+42del
ENST00000697151.1:c.1045+32_1045+42del ENSP00000513140.1:n.1045+32_1045+42del
ENST00000697152.1:c.799-19003_799-18993del ENSP00000513141.1:n.799-19003_799-18993de...
ENST00000697153.1:c.794+17104_794+17114del ENSP00000513142.1:n.794+17104_794+17114de...
ENST00000697154.1:c.955+17104_955+17114del ENSP00000513143.1:n.955+17104_955+17114de...
ENST00000697155.1:c.648+17104_648+17114del ENSP00000513144.1:n.648+17104_648+17114de...
ENST00000697156.1:c.1045+32_1045+42del ENSP00000513145.1:n.1045+32_1045+42del
ENST00000697157.1:c.899+32_899+42del ENSP00000513146.1:n.899+32_899+42del
ENST00000697158.1:c.888+32_888+42del ENSP00000513147.1:n.888+32_888+42del
ENST00000697159.1:c.738+32_738+42del ENSP00000513148.1:n.738+32_738+42del
ENST00000697160.1:c.955+17104_955+17114del ENSP00000513149.1:n.955+17104_955+17114de...
ENST00000697161.1:c.581+32_581+42del ENSP00000513150.1:n.581+32_581+42del
ENST00000697162.1:c.974+32_974+42del ENSP00000513151.1:n.974+32_974+42del
ENST00000697163.1:c.1045+32_1045+42del ENSP00000513152.1:n.1045+32_1045+42del
ENST00000697164.1:c.956-3345_956-3335del ENSP00000513153.1:n.956-3345_956-3335del
ENST00000697165.1:c.742+32_742+42del ENSP00000513154.1:n.742+32_742+42del
ENST00000697223.1:c.795-3345_795-3335del ENSP00000513190.1:n.795-3345_795-3335del
ENST00000697224.1:c.884+32_884+42del ENSP00000513191.1:n.884+32_884+42del
ENST00000697225.1:c.649-3345_649-3335del ENSP00000513192.1:n.649-3345_649-3335del
ENST00000697226.1:c.738+32_738+42del ENSP00000513193.1:n.738+32_738+42del
ENST00000697227.1:c.881+32_881+42del ENSP00000513194.1:n.881+32_881+42del
ENST00000697228.1:c.737+32_737+42del ENSP00000513195.1:n.737+32_737+42del
ENST00000697229.1:c.884+17104_884+17114del ENSP00000513196.1:n.884+17104_884+17114de...
ENST00000697230.1:c.956-3345_956-3335del ENSP00000513197.1:n.956-3345_956-3335del
ENST00000697231.1:c.951-3345_951-3335del ENSP00000513198.1:n.951-3345_951-3335del
ENST00000697232.1:c.974+32_974+42del ENSP00000513199.1:n.974+32_974+42del
ENST00000347310.10:c.1045+32_1045+42del MANE Select ENSP00000321345.5:n.1045+32_1045+42del
ENST00000637002.1:c.436+32_436+42del ENSP00000490340.1:n.436+32_436+42del
ENST00000347310.9:c.1045+32_1045+42del ENSP00000321345.5:n.1045+32_1045+42del
ENST00000395227.2:c.-59+17104_-59+17114del ENSP00000378652.2:n.-59+17104_-59+17114de...
ENST00000425614.3:c.280+32_280+42del ENSP00000387640.2:n.280+32_280+42del
ENST00000473881.2:c.190+17104_190+17114del ENSP00000486667.1:n.190+17104_190+17114de...
NM_144701.2:c.1045+32_1045+42del NP_653302.2:n.1045+32_1045+42del
XM_005270516.2:c.283+32_283+42del XP_005270573.1:n.283+32_283+42del
XM_011540789.1:c.1135+32_1135+42del XP_011539091.1:n.1135+32_1135+42del
XM_011540790.1:c.1045+32_1045+42del XP_011539092.1:n.1045+32_1045+42del
XM_011540791.1:c.1045+32_1045+42del XP_011539093.1:n.1045+32_1045+42del
XM_011540790.3:c.1045+32_1045+42del XP_011539092.1:n.1045+32_1045+42del
XM_011540791.3:c.1045+32_1045+42del XP_011539093.1:n.1045+32_1045+42del
XR_001736993.1:n.1228+32_1228+42del
NM_144701.3:c.1045+32_1045+42del MANE Select NP_653302.2:n.1045+32_1045+42del