Canonical Allele Identifier: CA2500306454
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259341del , CM000663.2:g.67259341del GRCh38
NC_000001.10:g.67725024del , CM000663.1:g.67725024del GRCh37
NC_000001.9:g.67497612del NCBI36
NG_011498.1:g.97856del

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*213del MANE Select ENSP00000321345.5:n.*213del
ENST00000347310.9:c.*213del ENSP00000321345.5:n.*213del
ENST00000395227.2:c.*213del ENSP00000378652.2:n.*213del
ENST00000473881.2:c.*929del ENSP00000486667.1:n.*929del
NM_144701.2:c.*213del NP_653302.2:n.*213del
XM_005270516.2:c.*213del XP_005270573.1:n.*213del
XM_011540789.1:c.*213del XP_011539091.1:n.*213del
XM_011540790.1:c.*213del XP_011539092.1:n.*213del
XM_011540791.1:c.*213del XP_011539093.1:n.*213del
XM_011540790.3:c.*213del XP_011539092.1:n.*213del
XM_011540791.3:c.*213del XP_011539093.1:n.*213del
NM_144701.3:c.*213del MANE Select NP_653302.2:n.*213del