Canonical Allele Identifier: CA2743979164
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258774_67258775insAACACACCCAACACA , CM000663.2:g.67258774_67258775insAACACACCCAACACA GRCh38
NC_000001.10:g.67724457_67724458insAACACACCCAACACA , CM000663.1:g.67724457_67724458insAACACACCCAACACA GRCh37
NC_000001.9:g.67497045_67497046insAACACACCCAACACA NCBI36
NG_011498.1:g.97289_97290insAACACACCCAACACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1375_1376insAACACACCCAACACA ENSP00000513138.1:n.1375_1376insAACACACCCAACACA
ENST00000697150.1:c.1433_1434insAACACACCCAACACA ENSP00000513139.1:n.1433_1434insAACACACCCAACACA
ENST00000697151.1:c.1366_1367insAACACACCCAACACA ENSP00000513140.1:n.1366_1367insAACACACCCAACACA
ENST00000697164.1:c.1446_1447insAACACACCCAACACA ENSP00000513153.1:p.Pro482_Val483insAsnThrProAsnThr
ENST00000697165.1:c.1233_1234insAACACACCCAACACA ENSP00000513154.1:p.Pro411_Val412insAsnThrProAsnThr
ENST00000347310.10:c.1536_1537insAACACACCCAACACA MANE Select ENSP00000321345.5:p.Pro512_Val513insAsnThrProAsnThr
ENST00000637002.1:c.927_928insAACACACCCAACACA ENSP00000490340.1:p.Pro309_Val310insAsnThrProAsnThr
ENST00000347310.9:c.1536_1537insAACACACCCAACACA ENSP00000321345.5:p.Pro512_Val513insAsnThrProAsnThr
ENST00000395227.2:c.330_331insAACACACCCAACACA ENSP00000378652.2:p.Pro110_Val111insAsnThrProAsnThr
ENST00000425614.3:c.771_772insAACACACCCAACACA ENSP00000387640.2:p.Pro257_Val258insAsnThrProAsnThr
ENST00000473881.2:c.*362_*363insAACACACCCAACACA ENSP00000486667.1:n.*362_*363insAACACACCCAACACA
NM_144701.2:c.1536_1537insAACACACCCAACACA NP_653302.2:p.Pro512_Val513insAsnThrProAsnThr
XM_005270516.2:c.774_775insAACACACCCAACACA XP_005270573.1:p.Pro258_Val259insAsnThrProAsnThr
XM_011540789.1:c.1626_1627insAACACACCCAACACA XP_011539091.1:p.Pro542_Val543insAsnThrProAsnThr
XM_011540790.1:c.1536_1537insAACACACCCAACACA XP_011539092.1:p.Pro512_Val513insAsnThrProAsnThr
XM_011540791.1:c.1536_1537insAACACACCCAACACA XP_011539093.1:p.Pro512_Val513insAsnThrProAsnThr
XM_011540790.3:c.1536_1537insAACACACCCAACACA XP_011539092.1:p.Pro512_Val513insAsnThrProAsnThr
XM_011540791.3:c.1536_1537insAACACACCCAACACA XP_011539093.1:p.Pro512_Val513insAsnThrProAsnThr
XR_001736993.1:n.1616_1617insAACACACCCAACACA
NM_144701.3:c.1536_1537insAACACACCCAACACA MANE Select NP_653302.2:p.Pro512_Val513insAsnThrProAsnThr