Canonical Allele Identifier: CA2569744557

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240213_67240214insGGCTACATGT , CM000663.2:g.67240213_67240214insGGCTACATGT	GRCh38
NC_000001.10:g.67705896_67705897insGGCTACATGT , CM000663.1:g.67705896_67705897insGGCTACATGT	GRCh37
NC_000001.9:g.67478484_67478485insGGCTACATGT	NCBI36
NG_011498.1:g.78728_78729insGGCTACATGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.956_957insGGCTACATGT	ENSP00000513137.1:n.956_957insGGCTACATGT
ENST00000697149.1:c.919_920insGGCTACATGT	ENSP00000513138.1:n.919_920insGGCTACATGT
ENST00000697150.1:c.1045+3411_1045+3412insGGCTACATGT	ENSP00000513139.1:n.1045+3411_1045+3412in...
ENST00000697151.1:c.1045+3411_1045+3412insGGCTACATGT	ENSP00000513140.1:n.1045+3411_1045+3412in...
ENST00000697152.1:c.799-15624_799-15623insGGCTACATGT	ENSP00000513141.1:n.799-15624_799-15623in...
ENST00000697153.1:c.795-15624_795-15623insGGCTACATGT	ENSP00000513142.1:n.795-15624_795-15623in...
ENST00000697154.1:c.956-18265_956-18264insGGCTACATGT	ENSP00000513143.1:n.956-18265_956-18264in...
ENST00000697155.1:c.649-18265_649-18264insGGCTACATGT	ENSP00000513144.1:n.649-18265_649-18264in...
ENST00000697156.1:c.1080_1081insGGCTACATGT	ENSP00000513145.1:p.Ile361GlyfsTer20
ENST00000697157.1:c.934_935insGGCTACATGT	ENSP00000513146.1:n.934_935insGGCTACATGT
ENST00000697158.1:c.923_924insGGCTACATGT	ENSP00000513147.1:n.923_924insGGCTACATGT
ENST00000697159.1:c.773_774insGGCTACATGT	ENSP00000513148.1:n.773_774insGGCTACATGT
ENST00000697160.1:c.956-15624_956-15623insGGCTACATGT	ENSP00000513149.1:n.956-15624_956-15623in...
ENST00000697161.1:c.616_617insGGCTACATGT	ENSP00000513150.1:n.616_617insGGCTACATGT
ENST00000697162.1:c.1009_1010insGGCTACATGT	ENSP00000513151.1:n.1009_1010insGGCTACATG...
ENST00000697163.1:c.1080_1081insGGCTACATGT	ENSP00000513152.1:p.Ile361GlyfsTer20
ENST00000697164.1:c.990_991insGGCTACATGT	ENSP00000513153.1:p.Ile331GlyfsTer20
ENST00000697165.1:c.777_778insGGCTACATGT	ENSP00000513154.1:p.Ile260GlyfsTer20
ENST00000697223.1:c.829_830insGGCTACATGT	ENSP00000513190.1:n.829_830insGGCTACATGT
ENST00000697224.1:c.884+3411_884+3412insGGCTACATGT	ENSP00000513191.1:n.884+3411_884+3412insG...
ENST00000697225.1:c.683_684insGGCTACATGT	ENSP00000513192.1:n.683_684insGGCTACATGT
ENST00000697226.1:c.738+3411_738+3412insGGCTACATGT	ENSP00000513193.1:n.738+3411_738+3412insG...
ENST00000697227.1:c.916_917insGGCTACATGT	ENSP00000513194.1:n.916_917insGGCTACATGT
ENST00000697228.1:c.772_773insGGCTACATGT	ENSP00000513195.1:n.772_773insGGCTACATGT
ENST00000697229.1:c.885-15624_885-15623insGGCTACATGT	ENSP00000513196.1:n.885-15624_885-15623in...
ENST00000697230.1:c.990_991insGGCTACATGT	ENSP00000513197.1:p.Ile331GlyfsTer20
ENST00000697231.1:c.985_986insGGCTACATGT	ENSP00000513198.1:n.985_986insGGCTACATGT
ENST00000697232.1:c.1009_1010insGGCTACATGT	ENSP00000513199.1:n.1009_1010insGGCTACATG...
ENST00000347310.10:c.1080_1081insGGCTACATGT MANE Select	ENSP00000321345.5:p.Ile361GlyfsTer20
ENST00000637002.1:c.471_472insGGCTACATGT	ENSP00000490340.1:p.Ile158GlyfsTer20
ENST00000347310.9:c.1080_1081insGGCTACATGT	ENSP00000321345.5:p.Ile361GlyfsTer20
ENST00000395227.2:c.-58-15624_-58-15623insGGCTACATGT	ENSP00000378652.2:n.-58-15624_-58-15623in...
ENST00000425614.3:c.315_316insGGCTACATGT	ENSP00000387640.2:p.Ile106GlyfsTer20
ENST00000473881.2:c.191-15624_191-15623insGGCTACATGT	ENSP00000486667.1:n.191-15624_191-15623in...
NM_144701.2:c.1080_1081insGGCTACATGT	NP_653302.2:p.Ile361GlyfsTer20
XM_005270516.2:c.318_319insGGCTACATGT	XP_005270573.1:p.Ile107GlyfsTer20
XM_011540789.1:c.1170_1171insGGCTACATGT	XP_011539091.1:p.Ile391GlyfsTer20
XM_011540790.1:c.1080_1081insGGCTACATGT	XP_011539092.1:p.Ile361GlyfsTer20
XM_011540791.1:c.1080_1081insGGCTACATGT	XP_011539093.1:p.Ile361GlyfsTer20
XM_011540790.3:c.1080_1081insGGCTACATGT	XP_011539092.1:p.Ile361GlyfsTer20
XM_011540791.3:c.1080_1081insGGCTACATGT	XP_011539093.1:p.Ile361GlyfsTer20
XR_001736993.1:n.1228+3411_1228+3412insGGCTACATGT
NM_144701.3:c.1080_1081insGGCTACATGT MANE Select	NP_653302.2:p.Ile361GlyfsTer20