Canonical Allele Identifier: CA23503582

Gene: IL23R

Linked Data

• dbSNP Id: rs386632079

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67255415_67255417delinsTTT , CM000663.2:g.67255415_67255417delinsTTT	GRCh38
NC_000001.10:g.67721098_67721100delinsTTT , CM000663.1:g.67721098_67721100delinsTTT	GRCh37
NC_000001.9:g.67493686_67493688delinsTTT	NCBI36
NG_011498.1:g.93930_93932delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.1025-422_1025-420delinsTTT	ENSP00000513137.1:n.1025-422_1025-420delinsTTT
ENST00000697149.1:c.988-422_988-420delinsTTT	ENSP00000513138.1:n.988-422_988-420delinsTTT
ENST00000697150.1:c.1046-422_1046-420delinsTTT	ENSP00000513139.1:n.1046-422_1046-420delinsTTT
ENST00000697151.1:c.1046-422_1046-420delinsTTT	ENSP00000513140.1:n.1046-422_1046-420delinsTTT
ENST00000697152.1:c.799-422_799-420delinsTTT	ENSP00000513141.1:n.799-422_799-420delinsTTT
ENST00000697153.1:c.795-422_795-420delinsTTT	ENSP00000513142.1:n.795-422_795-420delinsTTT
ENST00000697154.1:c.956-3063_956-3061delinsTTT	ENSP00000513143.1:n.956-3063_956-3061delinsTTT
ENST00000697155.1:c.649-3063_649-3061delinsTTT	ENSP00000513144.1:n.649-3063_649-3061delinsTTT
ENST00000697156.1:c.1282-422_1282-420delinsTTT	ENSP00000513145.1:n.1282-422_1282-420delinsTTT
ENST00000697157.1:c.1003-422_1003-420delinsTTT	ENSP00000513146.1:n.1003-422_1003-420delinsTTT
ENST00000697158.1:c.992-422_992-420delinsTTT	ENSP00000513147.1:n.992-422_992-420delinsTTT
ENST00000697159.1:c.842-422_842-420delinsTTT	ENSP00000513148.1:n.842-422_842-420delinsTTT
ENST00000697160.1:c.956-422_956-420delinsTTT	ENSP00000513149.1:n.956-422_956-420delinsTTT
ENST00000697161.1:c.685-422_685-420delinsTTT	ENSP00000513150.1:n.685-422_685-420delinsTTT
ENST00000697162.1:c.1078-422_1078-420delinsTTT	ENSP00000513151.1:n.1078-422_1078-420delinsTTT
ENST00000697163.1:c.1149-422_1149-420delinsTTT	ENSP00000513152.1:n.1149-422_1149-420delinsTTT
ENST00000697164.1:c.1059-422_1059-420delinsTTT	ENSP00000513153.1:n.1059-422_1059-420delinsTTT
ENST00000697165.1:c.846-422_846-420delinsTTT	ENSP00000513154.1:n.846-422_846-420delinsTTT
ENST00000697223.1:c.898-422_898-420delinsTTT	ENSP00000513190.1:n.898-422_898-420delinsTTT
ENST00000697224.1:c.885-422_885-420delinsTTT	ENSP00000513191.1:n.885-422_885-420delinsTTT
ENST00000697225.1:c.752-422_752-420delinsTTT	ENSP00000513192.1:n.752-422_752-420delinsTTT
ENST00000697226.1:c.739-422_739-420delinsTTT	ENSP00000513193.1:n.739-422_739-420delinsTTT
ENST00000697227.1:c.985-422_985-420delinsTTT	ENSP00000513194.1:n.985-422_985-420delinsTTT
ENST00000697228.1:c.841-422_841-420delinsTTT	ENSP00000513195.1:n.841-422_841-420delinsTTT
ENST00000697229.1:c.885-422_885-420delinsTTT	ENSP00000513196.1:n.885-422_885-420delinsTTT
ENST00000697230.1:c.1059-422_1059-420delinsTTT	ENSP00000513197.1:n.1059-422_1059-420delinsTTT
ENST00000697231.1:c.1054-422_1054-420delinsTTT	ENSP00000513198.1:n.1054-422_1054-420delinsTTT
ENST00000697232.1:c.1240-422_1240-420delinsTTT	ENSP00000513199.1:n.1240-422_1240-420delinsTTT
ENST00000347310.10:c.1149-422_1149-420delinsTTT MANE Select	ENSP00000321345.5:n.1149-422_1149-420delinsTTT
ENST00000637002.1:c.540-422_540-420delinsTTT	ENSP00000490340.1:n.540-422_540-420delinsTTT
ENST00000347310.9:c.1149-422_1149-420delinsTTT	ENSP00000321345.5:n.1149-422_1149-420delinsTTT
ENST00000395227.2:c.-58-422_-58-420delinsTTT	ENSP00000378652.2:n.-58-422_-58-420delinsTTT
ENST00000425614.3:c.384-422_384-420delinsTTT	ENSP00000387640.2:n.384-422_384-420delinsTTT
ENST00000473881.2:c.191-422_191-420delinsTTT	ENSP00000486667.1:n.191-422_191-420delinsTTT
NM_144701.2:c.1149-422_1149-420delinsTTT	NP_653302.2:n.1149-422_1149-420delinsTTT
XM_005270516.2:c.387-422_387-420delinsTTT	XP_005270573.1:n.387-422_387-420delinsTTT
XM_011540789.1:c.1239-422_1239-420delinsTTT	XP_011539091.1:n.1239-422_1239-420delinsTTT
XM_011540790.1:c.1149-422_1149-420delinsTTT	XP_011539092.1:n.1149-422_1149-420delinsTTT
XM_011540791.1:c.1149-422_1149-420delinsTTT	XP_011539093.1:n.1149-422_1149-420delinsTTT
XM_011540790.3:c.1149-422_1149-420delinsTTT	XP_011539092.1:n.1149-422_1149-420delinsTTT
XM_011540791.3:c.1149-422_1149-420delinsTTT	XP_011539093.1:n.1149-422_1149-420delinsTTT
XR_001736993.1:n.1229-422_1229-420delinsTTT
NM_144701.3:c.1149-422_1149-420delinsTTT MANE Select	NP_653302.2:n.1149-422_1149-420delinsTTT