Canonical Allele Identifier: CA1173043647

Gene: IL23R C1orf141

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67210025_67210026delinsCT , CM000663.2:g.67210025_67210026delinsCT	GRCh38
NC_000001.10:g.67675708_67675709delinsCT , CM000663.1:g.67675708_67675709delinsCT	GRCh37
NC_000001.9:g.67448296_67448297delinsCT	NCBI36
NG_011498.1:g.48540_48541delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.674+2970_674+2971delinsCT (IL23R)	ENSP00000513137.1:n.674+2970_674+2971delinsCT
ENST00000697149.1:c.637+2970_637+2971delinsCT (IL23R)	ENSP00000513138.1:n.637+2970_637+2971delinsCT
ENST00000697150.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513139.1:n.798+2970_798+2971delinsCT
ENST00000697151.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513140.1:n.798+2970_798+2971delinsCT
ENST00000697152.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513141.1:n.798+2970_798+2971delinsCT
ENST00000697153.1:c.637+2970_637+2971delinsCT (IL23R)	ENSP00000513142.1:n.637+2970_637+2971delinsCT
ENST00000697154.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513143.1:n.798+2970_798+2971delinsCT
ENST00000697155.1:c.492-9549_492-9548delinsCT (IL23R)	ENSP00000513144.1:n.492-9549_492-9548delinsCT
ENST00000697156.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513145.1:n.798+2970_798+2971delinsCT
ENST00000697157.1:c.652+9128_652+9129delinsCT (IL23R)	ENSP00000513146.1:n.652+9128_652+9129delinsCT
ENST00000697158.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513147.1:n.798+2970_798+2971delinsCT
ENST00000697159.1:c.492-9549_492-9548delinsCT (IL23R)	ENSP00000513148.1:n.492-9549_492-9548delinsCT
ENST00000697160.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513149.1:n.798+2970_798+2971delinsCT
ENST00000697161.1:c.492-26688_492-26687delinsCT (IL23R)	ENSP00000513150.1:n.492-26688_492-26687delinsCT
ENST00000697162.1:c.727+2970_727+2971delinsCT (IL23R)	ENSP00000513151.1:n.727+2970_727+2971delinsCT
ENST00000697163.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513152.1:n.798+2970_798+2971delinsCT
ENST00000697164.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513153.1:n.798+2970_798+2971delinsCT
ENST00000697165.1:c.652+9128_652+9129delinsCT (IL23R)	ENSP00000513154.1:n.652+9128_652+9129delinsCT
ENST00000697223.1:c.637+2970_637+2971delinsCT (IL23R)	ENSP00000513190.1:n.637+2970_637+2971delinsCT
ENST00000697224.1:c.637+2970_637+2971delinsCT (IL23R)	ENSP00000513191.1:n.637+2970_637+2971delinsCT
ENST00000697225.1:c.492-9549_492-9548delinsCT (IL23R)	ENSP00000513192.1:n.492-9549_492-9548delinsCT
ENST00000697226.1:c.492-9549_492-9548delinsCT (IL23R)	ENSP00000513193.1:n.492-9549_492-9548delinsCT
ENST00000697227.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513194.1:n.798+2970_798+2971delinsCT
ENST00000697228.1:c.647+9128_647+9129delinsCT (IL23R)	ENSP00000513195.1:n.647+9128_647+9129delinsCT
ENST00000697229.1:c.727+2970_727+2971delinsCT (IL23R)	ENSP00000513196.1:n.727+2970_727+2971delinsCT
ENST00000697230.1:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000513197.1:n.798+2970_798+2971delinsCT
ENST00000697231.1:c.793+2970_793+2971delinsCT (IL23R)	ENSP00000513198.1:n.793+2970_793+2971delinsCT
ENST00000697232.1:c.727+2970_727+2971delinsCT (IL23R)	ENSP00000513199.1:n.727+2970_727+2971delinsCT
ENST00000347310.10:c.798+2970_798+2971delinsCT (IL23R) MANE Select	ENSP00000321345.5:n.798+2970_798+2971delinsCT
ENST00000637002.1:c.189+2970_189+2971delinsCT (IL23R)	ENSP00000490340.1:n.189+2970_189+2971delinsCT
ENST00000347310.9:c.798+2970_798+2971delinsCT (IL23R)	ENSP00000321345.5:n.798+2970_798+2971delinsCT
ENST00000371007.6:c.-104+21820_-104+21821delinsAG (C1orf141)	ENSP00000360046.1:n.-104+21820_-104+21821delinsAG
ENST00000425614.3:c.33+2327_33+2328delinsCT (IL23R)	ENSP00000387640.2:n.33+2327_33+2328delinsCT
ENST00000448166.6:c.-104+21820_-104+21821delinsAG (C1orf141)	ENSP00000415519.2:n.-104+21820_-104+21821delinsAG
ENST00000473881.2:c.33+2327_33+2328delinsCT (IL23R)	ENSP00000486667.1:n.33+2327_33+2328delinsCT
NM_144701.2:c.798+2970_798+2971delinsCT (IL23R)	NP_653302.2:n.798+2970_798+2971delinsCT
XM_005270516.2:c.36+2970_36+2971delinsCT (IL23R)	XP_005270573.1:n.36+2970_36+2971delinsCT
XM_011540789.1:c.888+2970_888+2971delinsCT (IL23R)	XP_011539091.1:n.888+2970_888+2971delinsCT
XM_011540790.1:c.798+2970_798+2971delinsCT (IL23R)	XP_011539092.1:n.798+2970_798+2971delinsCT
XM_011540791.1:c.798+2970_798+2971delinsCT (IL23R)	XP_011539093.1:n.798+2970_798+2971delinsCT
XM_011540790.3:c.798+2970_798+2971delinsCT (IL23R)	XP_011539092.1:n.798+2970_798+2971delinsCT
XM_011540791.3:c.798+2970_798+2971delinsCT (IL23R)	XP_011539093.1:n.798+2970_798+2971delinsCT
XR_001736993.1:n.981+2970_981+2971delinsCT (IL23R)
NM_144701.3:c.798+2970_798+2971delinsCT (IL23R) MANE Select	NP_653302.2:n.798+2970_798+2971delinsCT