Canonical Allele Identifier: CA1173064386

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259207_67259217delinsCTGCCTCTTTT , CM000663.2:g.67259207_67259217delinsCTGCCTCTTTT	GRCh38
NC_000001.10:g.67724890_67724900delinsCTGCCTCTTTT , CM000663.1:g.67724890_67724900delinsCTGCCTCTTTT	GRCh37
NC_000001.9:g.67497478_67497488delinsCTGCCTCTTTT	NCBI36
NG_011498.1:g.97722_97732delinsCTGCCTCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*79_*89delinsCTGCCTCTTTT MANE Select	ENSP00000321345.5:n.*79_*89delinsCTGCCTCTTTT
ENST00000347310.9:c.*79_*89delinsCTGCCTCTTTT	ENSP00000321345.5:n.*79_*89delinsCTGCCTCTTTT
ENST00000395227.2:c.*79_*89delinsCTGCCTCTTTT	ENSP00000378652.2:n.*79_*89delinsCTGCCTCTTTT
ENST00000425614.3:c.*79_*89delinsCTGCCTCTTTT	ENSP00000387640.2:n.*79_*89delinsCTGCCTCTTTT
ENST00000473881.2:c.*795_*805delinsCTGCCTCTTTT	ENSP00000486667.1:n.*795_*805delinsCTGCCTCTTTT
NM_144701.2:c.*79_*89delinsCTGCCTCTTTT	NP_653302.2:n.*79_*89delinsCTGCCTCTTTT
XM_005270516.2:c.*79_*89delinsCTGCCTCTTTT	XP_005270573.1:n.*79_*89delinsCTGCCTCTTTT
XM_011540789.1:c.*79_*89delinsCTGCCTCTTTT	XP_011539091.1:n.*79_*89delinsCTGCCTCTTTT
XM_011540790.1:c.*79_*89delinsCTGCCTCTTTT	XP_011539092.1:n.*79_*89delinsCTGCCTCTTTT
XM_011540791.1:c.*79_*89delinsCTGCCTCTTTT	XP_011539093.1:n.*79_*89delinsCTGCCTCTTTT
XM_011540790.3:c.*79_*89delinsCTGCCTCTTTT	XP_011539092.1:n.*79_*89delinsCTGCCTCTTTT
XM_011540791.3:c.*79_*89delinsCTGCCTCTTTT	XP_011539093.1:n.*79_*89delinsCTGCCTCTTTT
NM_144701.3:c.*79_*89delinsCTGCCTCTTTT MANE Select	NP_653302.2:n.*79_*89delinsCTGCCTCTTTT