Canonical Allele Identifier: CA1173064559
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259589_67259594delinsACAGCT , CM000663.2:g.67259589_67259594delinsACAGCT GRCh38
NC_000001.10:g.67725272_67725277delinsACAGCT , CM000663.1:g.67725272_67725277delinsACAGCT GRCh37
NC_000001.9:g.67497860_67497865delinsACAGCT NCBI36
NG_011498.1:g.98104_98109delinsACAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000347310.10:c.*461_*466delinsACAGCT MANE Select ENSP00000321345.5:n.*461_*466delinsACAGCT
ENST00000347310.9:c.*461_*466delinsACAGCT ENSP00000321345.5:n.*461_*466delinsACAGCT
ENST00000395227.2:c.*461_*466delinsACAGCT ENSP00000378652.2:n.*461_*466delinsACAGCT
ENST00000473881.2:c.*1177_*1182delinsACAGCT ENSP00000486667.1:n.*1177_*1182delinsACAGCT
NM_144701.2:c.*461_*466delinsACAGCT NP_653302.2:n.*461_*466delinsACAGCT
XM_005270516.2:c.*461_*466delinsACAGCT XP_005270573.1:n.*461_*466delinsACAGCT
XM_011540789.1:c.*461_*466delinsACAGCT XP_011539091.1:n.*461_*466delinsACAGCT
XM_011540790.1:c.*461_*466delinsACAGCT XP_011539092.1:n.*461_*466delinsACAGCT
XM_011540791.1:c.*461_*466delinsACAGCT XP_011539093.1:n.*461_*466delinsACAGCT
XM_011540790.3:c.*461_*466delinsACAGCT XP_011539092.1:n.*461_*466delinsACAGCT
XM_011540791.3:c.*461_*466delinsACAGCT XP_011539093.1:n.*461_*466delinsACAGCT
NM_144701.3:c.*461_*466delinsACAGCT MANE Select NP_653302.2:n.*461_*466delinsACAGCT