Canonical Allele Identifier: CA523607599
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259226_67259227insAAAAAAAAAA , CM000663.2:g.67259226_67259227insAAAAAAAAAA GRCh38
NC_000001.10:g.67724909_67724910insAAAAAAAAAA , CM000663.1:g.67724909_67724910insAAAAAAAAAA GRCh37
NC_000001.9:g.67497497_67497498insAAAAAAAAAA NCBI36
NG_011498.1:g.97741_97742insAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000347310.10:c.*98_*99insAAAAAAAAAA MANE Select ENSP00000321345.5:n.*98_*99insAAAAAAAAAA
ENST00000347310.9:c.*98_*99insAAAAAAAAAA ENSP00000321345.5:n.*98_*99insAAAAAAAAAA
ENST00000395227.2:c.*98_*99insAAAAAAAAAA ENSP00000378652.2:n.*98_*99insAAAAAAAAAA
ENST00000425614.3:c.*98_*99insAAAAAAAAAA ENSP00000387640.2:n.*98_*99insAAAAAAAAAA
ENST00000473881.2:c.*814_*815insAAAAAAAAAA ENSP00000486667.1:n.*814_*815insAAAAAAAAAA
NM_144701.2:c.*98_*99insAAAAAAAAAA NP_653302.2:n.*98_*99insAAAAAAAAAA
XM_005270516.2:c.*98_*99insAAAAAAAAAA XP_005270573.1:n.*98_*99insAAAAAAAAAA
XM_011540789.1:c.*98_*99insAAAAAAAAAA XP_011539091.1:n.*98_*99insAAAAAAAAAA
XM_011540790.1:c.*98_*99insAAAAAAAAAA XP_011539092.1:n.*98_*99insAAAAAAAAAA
XM_011540791.1:c.*98_*99insAAAAAAAAAA XP_011539093.1:n.*98_*99insAAAAAAAAAA
XM_011540790.3:c.*98_*99insAAAAAAAAAA XP_011539092.1:n.*98_*99insAAAAAAAAAA
XM_011540791.3:c.*98_*99insAAAAAAAAAA XP_011539093.1:n.*98_*99insAAAAAAAAAA
NM_144701.3:c.*98_*99insAAAAAAAAAA MANE Select NP_653302.2:n.*98_*99insAAAAAAAAAA