Canonical Allele Identifier: CA899608
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs745976353

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67168099_67168100del , CM000663.2:g.67168099_67168100del GRCh38
NC_000001.10:g.67633782_67633783del , CM000663.1:g.67633782_67633783del GRCh37
NC_000001.9:g.67406370_67406371del NCBI36
NG_011498.1:g.6614_6615del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697222.1:c.-22_-21del (IL23R) ENSP00000513189.1:n.-22_-21del
ENST00000347310.10:c.-22_-21del (IL23R) MANE Select ENSP00000321345.5:n.-22_-21del
ENST00000637002.1:c.-626_-625del (IL23R) ENSP00000490340.1:n.-626_-625del
ENST00000347310.9:c.-22_-21del (IL23R) ENSP00000321345.5:n.-22_-21del
ENST00000371007.6:c.-103-36872_-103-36871del (C1orf141) ENSP00000360046.1:n.-103-36872_-103-36871del
ENST00000448166.6:c.-103-36872_-103-36871del (C1orf141) ENSP00000415519.2:n.-103-36872_-103-36871del
NM_144701.2:c.-22_-21del (IL23R) NP_653302.2:n.-22_-21del
XM_011540789.1:c.69_70del (IL23R) XP_011539091.1:p.Asn23LysfsTer?
XM_011540790.1:c.-22_-21del (IL23R) XP_011539092.1:n.-22_-21del
XM_011540791.1:c.-22_-21del (IL23R) XP_011539093.1:n.-22_-21del
XM_011540790.3:c.-22_-21del (IL23R) XP_011539092.1:n.-22_-21del
XM_011540791.3:c.-22_-21del (IL23R) XP_011539093.1:n.-22_-21del
XR_001736993.1:n.162_163del (IL23R)
NM_144701.3:c.-22_-21del (IL23R) MANE Select NP_653302.2:n.-22_-21del