Canonical Allele Identifier: CA1173056552

Gene: IL23R

Linked Data

• ClinVar Variation Id: 1021370
• ClinVar RCV Id: RCV001321122
• dbSNP Id: rs1651763913

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240249_67240250delinsCT , CM000663.2:g.67240249_67240250delinsCT	GRCh38
NC_000001.10:g.67705932_67705933delinsCT , CM000663.1:g.67705932_67705933delinsCT	GRCh37
NC_000001.9:g.67478520_67478521delinsCT	NCBI36
NG_011498.1:g.78764_78765delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.992_993delinsCT	ENSP00000513137.1:n.992_993delinsCT
ENST00000697149.1:c.955_956delinsCT	ENSP00000513138.1:n.955_956delinsCT
ENST00000697150.1:c.1045+3447_1045+3448delinsCT	ENSP00000513139.1:n.1045+3447_1045+3448delinsCT
ENST00000697151.1:c.1045+3447_1045+3448delinsCT	ENSP00000513140.1:n.1045+3447_1045+3448delinsCT
ENST00000697152.1:c.799-15588_799-15587delinsCT	ENSP00000513141.1:n.799-15588_799-15587delinsCT
ENST00000697153.1:c.795-15588_795-15587delinsCT	ENSP00000513142.1:n.795-15588_795-15587delinsCT
ENST00000697154.1:c.956-18229_956-18228delinsCT	ENSP00000513143.1:n.956-18229_956-18228delinsCT
ENST00000697155.1:c.649-18229_649-18228delinsCT	ENSP00000513144.1:n.649-18229_649-18228delinsCT
ENST00000697156.1:c.1116_1117delinsCT	ENSP00000513145.1:p.Leu372_Ile373delinsPhePhe
ENST00000697157.1:c.970_971delinsCT	ENSP00000513146.1:n.970_971delinsCT
ENST00000697158.1:c.959_960delinsCT	ENSP00000513147.1:n.959_960delinsCT
ENST00000697159.1:c.809_810delinsCT	ENSP00000513148.1:n.809_810delinsCT
ENST00000697160.1:c.956-15588_956-15587delinsCT	ENSP00000513149.1:n.956-15588_956-15587delinsCT
ENST00000697161.1:c.652_653delinsCT	ENSP00000513150.1:n.652_653delinsCT
ENST00000697162.1:c.1045_1046delinsCT	ENSP00000513151.1:n.1045_1046delinsCT
ENST00000697163.1:c.1116_1117delinsCT	ENSP00000513152.1:p.Leu372_Ile373delinsPhePhe
ENST00000697164.1:c.1026_1027delinsCT	ENSP00000513153.1:p.Leu342_Ile343delinsPhePhe
ENST00000697165.1:c.813_814delinsCT	ENSP00000513154.1:p.Leu271_Ile272delinsPhePhe
ENST00000697223.1:c.865_866delinsCT	ENSP00000513190.1:n.865_866delinsCT
ENST00000697224.1:c.884+3447_884+3448delinsCT	ENSP00000513191.1:n.884+3447_884+3448delinsCT
ENST00000697225.1:c.719_720delinsCT	ENSP00000513192.1:n.719_720delinsCT
ENST00000697226.1:c.738+3447_738+3448delinsCT	ENSP00000513193.1:n.738+3447_738+3448delinsCT
ENST00000697227.1:c.952_953delinsCT	ENSP00000513194.1:n.952_953delinsCT
ENST00000697228.1:c.808_809delinsCT	ENSP00000513195.1:n.808_809delinsCT
ENST00000697229.1:c.885-15588_885-15587delinsCT	ENSP00000513196.1:n.885-15588_885-15587delinsCT
ENST00000697230.1:c.1026_1027delinsCT	ENSP00000513197.1:p.Leu342_Ile343delinsPhePhe
ENST00000697231.1:c.1021_1022delinsCT	ENSP00000513198.1:n.1021_1022delinsCT
ENST00000697232.1:c.1045_1046delinsCT	ENSP00000513199.1:n.1045_1046delinsCT
ENST00000347310.10:c.1116_1117delinsCT MANE Select	ENSP00000321345.5:p.Leu372_Ile373delinsPhePhe
ENST00000637002.1:c.507_508delinsCT	ENSP00000490340.1:p.Leu169_Ile170delinsPhePhe
ENST00000347310.9:c.1116_1117delinsCT	ENSP00000321345.5:p.Leu372_Ile373delinsPhePhe
ENST00000395227.2:c.-58-15588_-58-15587delinsCT	ENSP00000378652.2:n.-58-15588_-58-15587delinsCT
ENST00000425614.3:c.351_352delinsCT	ENSP00000387640.2:p.Leu117_Ile118delinsPhePhe
ENST00000473881.2:c.191-15588_191-15587delinsCT	ENSP00000486667.1:n.191-15588_191-15587delinsCT
NM_144701.2:c.1116_1117delinsCT	NP_653302.2:p.Leu372_Ile373delinsPhePhe
XM_005270516.2:c.354_355delinsCT	XP_005270573.1:p.Leu118_Ile119delinsPhePhe
XM_011540789.1:c.1206_1207delinsCT	XP_011539091.1:p.Leu402_Ile403delinsPhePhe
XM_011540790.1:c.1116_1117delinsCT	XP_011539092.1:p.Leu372_Ile373delinsPhePhe
XM_011540791.1:c.1116_1117delinsCT	XP_011539093.1:p.Leu372_Ile373delinsPhePhe
XM_011540790.3:c.1116_1117delinsCT	XP_011539092.1:p.Leu372_Ile373delinsPhePhe
XM_011540791.3:c.1116_1117delinsCT	XP_011539093.1:p.Leu372_Ile373delinsPhePhe
XR_001736993.1:n.1228+3447_1228+3448delinsCT
NM_144701.3:c.1116_1117delinsCT MANE Select	NP_653302.2:p.Leu372_Ile373delinsPhePhe