Canonical Allele Identifier: CA1173042442

Gene: IL23R C1orf141

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67206961T= , CM000663.2:g.67206961T=	GRCh38
NC_000001.10:g.67672644T= , CM000663.1:g.67672644T=	GRCh37
NC_000001.9:g.67445232T=	NCBI36
NG_011498.1:g.45476T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.580T= (IL23R)	ENSP00000513137.1:n.580T=
ENST00000697149.1:c.543T= (IL23R)	ENSP00000513138.1:n.543T=
ENST00000697150.1:c.704T= (IL23R)	ENSP00000513139.1:p.Val235=
ENST00000697151.1:c.704T= (IL23R)	ENSP00000513140.1:p.Val235=
ENST00000697152.1:c.704T= (IL23R)	ENSP00000513141.1:p.Val235=
ENST00000697153.1:c.543T= (IL23R)	ENSP00000513142.1:n.543T=
ENST00000697154.1:c.704T= (IL23R)	ENSP00000513143.1:p.Val235=
ENST00000697155.1:c.492-12613T= (IL23R)	ENSP00000513144.1:n.492-12613T=
ENST00000697156.1:c.704T= (IL23R)	ENSP00000513145.1:p.Val235=
ENST00000697157.1:c.652+6064T= (IL23R)	ENSP00000513146.1:n.652+6064T=
ENST00000697158.1:c.704T= (IL23R)	ENSP00000513147.1:p.Val235=
ENST00000697159.1:c.492-12613T= (IL23R)	ENSP00000513148.1:n.492-12613T=
ENST00000697160.1:c.704T= (IL23R)	ENSP00000513149.1:p.Val235=
ENST00000697161.1:c.491+24002T= (IL23R)	ENSP00000513150.1:n.491+24002T=
ENST00000697162.1:c.633T= (IL23R)	ENSP00000513151.1:n.633T=
ENST00000697163.1:c.704T= (IL23R)	ENSP00000513152.1:p.Val235=
ENST00000697164.1:c.704T= (IL23R)	ENSP00000513153.1:p.Val235=
ENST00000697165.1:c.652+6064T= (IL23R)	ENSP00000513154.1:n.652+6064T=
ENST00000697223.1:c.543T= (IL23R)	ENSP00000513190.1:n.543T=
ENST00000697224.1:c.543T= (IL23R)	ENSP00000513191.1:n.543T=
ENST00000697225.1:c.492-12613T= (IL23R)	ENSP00000513192.1:n.492-12613T=
ENST00000697226.1:c.492-12613T= (IL23R)	ENSP00000513193.1:n.492-12613T=
ENST00000697227.1:c.704T= (IL23R)	ENSP00000513194.1:p.Val235=
ENST00000697228.1:c.647+6064T= (IL23R)	ENSP00000513195.1:n.647+6064T=
ENST00000697229.1:c.633T= (IL23R)	ENSP00000513196.1:n.633T=
ENST00000697230.1:c.704T= (IL23R)	ENSP00000513197.1:p.Val235=
ENST00000697231.1:c.699T= (IL23R)	ENSP00000513198.1:n.699T=
ENST00000697232.1:c.633T= (IL23R)	ENSP00000513199.1:n.633T=
ENST00000347310.10:c.704T= (IL23R) MANE Select	ENSP00000321345.5:p.Val235=
ENST00000637002.1:c.95T= (IL23R)	ENSP00000490340.1:p.Val32=
ENST00000347310.9:c.704T= (IL23R)	ENSP00000321345.5:p.Val235=
ENST00000371007.6:c.-104+24885A= (C1orf141)	ENSP00000360046.1:n.-104+24885A=
ENST00000448166.6:c.-104+24885A= (C1orf141)	ENSP00000415519.2:n.-104+24885A=
NM_144701.2:c.704T= (IL23R)	NP_653302.2:p.Val235=
XM_005270516.2:c.-59T= (IL23R)	XP_005270573.1:n.-59T=
XM_011540789.1:c.794T= (IL23R)	XP_011539091.1:p.Val265=
XM_011540790.1:c.704T= (IL23R)	XP_011539092.1:p.Val235=
XM_011540791.1:c.704T= (IL23R)	XP_011539093.1:p.Val235=
XM_011540790.3:c.704T= (IL23R)	XP_011539092.1:p.Val235=
XM_011540791.3:c.704T= (IL23R)	XP_011539093.1:p.Val235=
XR_001736993.1:n.887T= (IL23R)
NM_144701.3:c.704T= (IL23R) MANE Select	NP_653302.2:p.Val235=