Canonical Allele Identifier: CA1173064454
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259385_67259389delinsTAAGA , CM000663.2:g.67259385_67259389delinsTAAGA GRCh38
NC_000001.10:g.67725068_67725072delinsTAAGA , CM000663.1:g.67725068_67725072delinsTAAGA GRCh37
NC_000001.9:g.67497656_67497660delinsTAAGA NCBI36
NG_011498.1:g.97900_97904delinsTAAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*257_*261delinsTAAGA MANE Select ENSP00000321345.5:n.*257_*261delinsTAAGA
ENST00000347310.9:c.*257_*261delinsTAAGA ENSP00000321345.5:n.*257_*261delinsTAAGA
ENST00000395227.2:c.*257_*261delinsTAAGA ENSP00000378652.2:n.*257_*261delinsTAAGA
ENST00000473881.2:c.*973_*977delinsTAAGA ENSP00000486667.1:n.*973_*977delinsTAAGA
NM_144701.2:c.*257_*261delinsTAAGA NP_653302.2:n.*257_*261delinsTAAGA
XM_005270516.2:c.*257_*261delinsTAAGA XP_005270573.1:n.*257_*261delinsTAAGA
XM_011540789.1:c.*257_*261delinsTAAGA XP_011539091.1:n.*257_*261delinsTAAGA
XM_011540790.1:c.*257_*261delinsTAAGA XP_011539092.1:n.*257_*261delinsTAAGA
XM_011540791.1:c.*257_*261delinsTAAGA XP_011539093.1:n.*257_*261delinsTAAGA
XM_011540790.3:c.*257_*261delinsTAAGA XP_011539092.1:n.*257_*261delinsTAAGA
XM_011540791.3:c.*257_*261delinsTAAGA XP_011539093.1:n.*257_*261delinsTAAGA
NM_144701.3:c.*257_*261delinsTAAGA MANE Select NP_653302.2:n.*257_*261delinsTAAGA