Canonical Allele Identifier: CA1173064405
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259257_67259259delinsCAT , CM000663.2:g.67259257_67259259delinsCAT GRCh38
NC_000001.10:g.67724940_67724942delinsCAT , CM000663.1:g.67724940_67724942delinsCAT GRCh37
NC_000001.9:g.67497528_67497530delinsCAT NCBI36
NG_011498.1:g.97772_97774delinsCAT

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*129_*131delinsCAT MANE Select ENSP00000321345.5:n.*129_*131delinsCAT
ENST00000347310.9:c.*129_*131delinsCAT ENSP00000321345.5:n.*129_*131delinsCAT
ENST00000395227.2:c.*129_*131delinsCAT ENSP00000378652.2:n.*129_*131delinsCAT
ENST00000473881.2:c.*845_*847delinsCAT ENSP00000486667.1:n.*845_*847delinsCAT
NM_144701.2:c.*129_*131delinsCAT NP_653302.2:n.*129_*131delinsCAT
XM_005270516.2:c.*129_*131delinsCAT XP_005270573.1:n.*129_*131delinsCAT
XM_011540789.1:c.*129_*131delinsCAT XP_011539091.1:n.*129_*131delinsCAT
XM_011540790.1:c.*129_*131delinsCAT XP_011539092.1:n.*129_*131delinsCAT
XM_011540791.1:c.*129_*131delinsCAT XP_011539093.1:n.*129_*131delinsCAT
XM_011540790.3:c.*129_*131delinsCAT XP_011539092.1:n.*129_*131delinsCAT
XM_011540791.3:c.*129_*131delinsCAT XP_011539093.1:n.*129_*131delinsCAT
NM_144701.3:c.*129_*131delinsCAT MANE Select NP_653302.2:n.*129_*131delinsCAT