Canonical Allele Identifier: CA1173064382
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259196_67259197delinsGA , CM000663.2:g.67259196_67259197delinsGA GRCh38
NC_000001.10:g.67724879_67724880delinsGA , CM000663.1:g.67724879_67724880delinsGA GRCh37
NC_000001.9:g.67497467_67497468delinsGA NCBI36
NG_011498.1:g.97711_97712delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*68_*69delinsGA MANE Select ENSP00000321345.5:n.*68_*69delinsGA
ENST00000347310.9:c.*68_*69delinsGA ENSP00000321345.5:n.*68_*69delinsGA
ENST00000395227.2:c.*68_*69delinsGA ENSP00000378652.2:n.*68_*69delinsGA
ENST00000425614.3:c.*68_*69delinsGA ENSP00000387640.2:n.*68_*69delinsGA
ENST00000473881.2:c.*784_*785delinsGA ENSP00000486667.1:n.*784_*785delinsGA
NM_144701.2:c.*68_*69delinsGA NP_653302.2:n.*68_*69delinsGA
XM_005270516.2:c.*68_*69delinsGA XP_005270573.1:n.*68_*69delinsGA
XM_011540789.1:c.*68_*69delinsGA XP_011539091.1:n.*68_*69delinsGA
XM_011540790.1:c.*68_*69delinsGA XP_011539092.1:n.*68_*69delinsGA
XM_011540791.1:c.*68_*69delinsGA XP_011539093.1:n.*68_*69delinsGA
XM_011540790.3:c.*68_*69delinsGA XP_011539092.1:n.*68_*69delinsGA
XM_011540791.3:c.*68_*69delinsGA XP_011539093.1:n.*68_*69delinsGA
NM_144701.3:c.*68_*69delinsGA MANE Select NP_653302.2:n.*68_*69delinsGA