Canonical Allele Identifier: CA1173064430
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259317_67259319delinsCAT , CM000663.2:g.67259317_67259319delinsCAT GRCh38
NC_000001.10:g.67725000_67725002delinsCAT , CM000663.1:g.67725000_67725002delinsCAT GRCh37
NC_000001.9:g.67497588_67497590delinsCAT NCBI36
NG_011498.1:g.97832_97834delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000347310.10:c.*189_*191delinsCAT MANE Select ENSP00000321345.5:n.*189_*191delinsCAT
ENST00000347310.9:c.*189_*191delinsCAT ENSP00000321345.5:n.*189_*191delinsCAT
ENST00000395227.2:c.*189_*191delinsCAT ENSP00000378652.2:n.*189_*191delinsCAT
ENST00000473881.2:c.*905_*907delinsCAT ENSP00000486667.1:n.*905_*907delinsCAT
NM_144701.2:c.*189_*191delinsCAT NP_653302.2:n.*189_*191delinsCAT
XM_005270516.2:c.*189_*191delinsCAT XP_005270573.1:n.*189_*191delinsCAT
XM_011540789.1:c.*189_*191delinsCAT XP_011539091.1:n.*189_*191delinsCAT
XM_011540790.1:c.*189_*191delinsCAT XP_011539092.1:n.*189_*191delinsCAT
XM_011540791.1:c.*189_*191delinsCAT XP_011539093.1:n.*189_*191delinsCAT
XM_011540790.3:c.*189_*191delinsCAT XP_011539092.1:n.*189_*191delinsCAT
XM_011540791.3:c.*189_*191delinsCAT XP_011539093.1:n.*189_*191delinsCAT
NM_144701.3:c.*189_*191delinsCAT MANE Select NP_653302.2:n.*189_*191delinsCAT