Canonical Allele Identifier: CA1173051942
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67228736T= , CM000663.2:g.67228736T= GRCh38
NC_000001.10:g.67694419T= , CM000663.1:g.67694419T= GRCh37
NC_000001.9:g.67467007T= NCBI36
NG_011498.1:g.67251T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697148.1:c.832-7977T= (IL23R) ENSP00000513137.1:n.832-7977T=
ENST00000697149.1:c.795-7977T= (IL23R) ENSP00000513138.1:n.795-7977T=
ENST00000697150.1:c.956-7977T= (IL23R) ENSP00000513139.1:n.956-7977T=
ENST00000697151.1:c.956-7977T= (IL23R) ENSP00000513140.1:n.956-7977T=
ENST00000697152.1:c.798+21681T= (IL23R) ENSP00000513141.1:n.798+21681T=
ENST00000697153.1:c.794+9006T= (IL23R) ENSP00000513142.1:n.794+9006T=
ENST00000697154.1:c.955+9006T= (IL23R) ENSP00000513143.1:n.955+9006T=
ENST00000697155.1:c.648+9006T= (IL23R) ENSP00000513144.1:n.648+9006T=
ENST00000697156.1:c.956-7977T= (IL23R) ENSP00000513145.1:n.956-7977T=
ENST00000697157.1:c.810-7977T= (IL23R) ENSP00000513146.1:n.810-7977T=
ENST00000697158.1:c.799-7977T= (IL23R) ENSP00000513147.1:n.799-7977T=
ENST00000697159.1:c.649-7977T= (IL23R) ENSP00000513148.1:n.649-7977T=
ENST00000697160.1:c.955+9006T= (IL23R) ENSP00000513149.1:n.955+9006T=
ENST00000697161.1:c.492-7977T= (IL23R) ENSP00000513150.1:n.492-7977T=
ENST00000697162.1:c.885-7977T= (IL23R) ENSP00000513151.1:n.885-7977T=
ENST00000697163.1:c.956-7977T= (IL23R) ENSP00000513152.1:n.956-7977T=
ENST00000697164.1:c.955+9006T= (IL23R) ENSP00000513153.1:n.955+9006T=
ENST00000697165.1:c.653-7977T= (IL23R) ENSP00000513154.1:n.653-7977T=
ENST00000697223.1:c.794+9006T= (IL23R) ENSP00000513190.1:n.794+9006T=
ENST00000697224.1:c.795-7977T= (IL23R) ENSP00000513191.1:n.795-7977T=
ENST00000697225.1:c.648+9006T= (IL23R) ENSP00000513192.1:n.648+9006T=
ENST00000697226.1:c.649-7977T= (IL23R) ENSP00000513193.1:n.649-7977T=
ENST00000697227.1:c.867-8052T= (IL23R) ENSP00000513194.1:n.867-8052T=
ENST00000697228.1:c.648-7977T= (IL23R) ENSP00000513195.1:n.648-7977T=
ENST00000697229.1:c.884+9006T= (IL23R) ENSP00000513196.1:n.884+9006T=
ENST00000697230.1:c.955+9006T= (IL23R) ENSP00000513197.1:n.955+9006T=
ENST00000697231.1:c.950+9006T= (IL23R) ENSP00000513198.1:n.950+9006T=
ENST00000697232.1:c.885-7977T= (IL23R) ENSP00000513199.1:n.885-7977T=
ENST00000347310.10:c.956-7977T= (IL23R) MANE Select ENSP00000321345.5:n.956-7977T=
ENST00000637002.1:c.347-7977T= (IL23R) ENSP00000490340.1:n.347-7977T=
ENST00000347310.9:c.956-7977T= (IL23R) ENSP00000321345.5:n.956-7977T=
ENST00000371007.6:c.-104+3110A= (C1orf141) ENSP00000360046.1:n.-104+3110A=
ENST00000395227.2:c.-59+9006T= (IL23R) ENSP00000378652.2:n.-59+9006T=
ENST00000425614.3:c.191-7977T= (IL23R) ENSP00000387640.2:n.191-7977T=
ENST00000448166.6:c.-104+3110A= (C1orf141) ENSP00000415519.2:n.-104+3110A=
ENST00000473881.2:c.190+9006T= (IL23R) ENSP00000486667.1:n.190+9006T=
NM_144701.2:c.956-7977T= (IL23R) NP_653302.2:n.956-7977T=
XM_005270516.2:c.194-7977T= (IL23R) XP_005270573.1:n.194-7977T=
XM_011540789.1:c.1046-7977T= (IL23R) XP_011539091.1:n.1046-7977T=
XM_011540790.1:c.956-7977T= (IL23R) XP_011539092.1:n.956-7977T=
XM_011540791.1:c.956-7977T= (IL23R) XP_011539093.1:n.956-7977T=
XM_011540790.3:c.956-7977T= (IL23R) XP_011539092.1:n.956-7977T=
XM_011540791.3:c.956-7977T= (IL23R) XP_011539093.1:n.956-7977T=
XR_001736993.1:n.1139-7977T= (IL23R)
NM_144701.3:c.956-7977T= (IL23R) MANE Select NP_653302.2:n.956-7977T=