Canonical Allele Identifier: CA2646126150
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259448del , CM000663.2:g.67259448del GRCh38
NC_000001.10:g.67725131del , CM000663.1:g.67725131del GRCh37
NC_000001.9:g.67497719del NCBI36
NG_011498.1:g.97963del

Transcript Alleles

HGVS Amino-acid Change
ENST00000347310.10:c.*320del MANE Select ENSP00000321345.5:n.*320del
ENST00000347310.9:c.*320del ENSP00000321345.5:n.*320del
ENST00000395227.2:c.*320del ENSP00000378652.2:n.*320del
ENST00000473881.2:c.*1036del ENSP00000486667.1:n.*1036del
NM_144701.2:c.*320del NP_653302.2:n.*320del
XM_005270516.2:c.*320del XP_005270573.1:n.*320del
XM_011540789.1:c.*320del XP_011539091.1:n.*320del
XM_011540790.1:c.*320del XP_011539092.1:n.*320del
XM_011540791.1:c.*320del XP_011539093.1:n.*320del
XM_011540790.3:c.*320del XP_011539092.1:n.*320del
XM_011540791.3:c.*320del XP_011539093.1:n.*320del
NM_144701.3:c.*320del MANE Select NP_653302.2:n.*320del