Canonical Allele Identifier: CA1173025846

Gene: IL23R C1orf141

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67168036T= , CM000663.2:g.67168036T=	GRCh38
NC_000001.10:g.67633719T= , CM000663.1:g.67633719T=	GRCh37
NC_000001.9:g.67406307T=	NCBI36
NG_011498.1:g.6551T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697222.1:c.-29-56T= (IL23R)	ENSP00000513189.1:n.-29-56T=
ENST00000347310.10:c.-29-56T= (IL23R) MANE Select	ENSP00000321345.5:n.-29-56T=
ENST00000637002.1:c.-633-56T= (IL23R)	ENSP00000490340.1:n.-633-56T=
ENST00000347310.9:c.-29-56T= (IL23R)	ENSP00000321345.5:n.-29-56T=
ENST00000371007.6:c.-103-36809A= (C1orf141)	ENSP00000360046.1:n.-103-36809A=
ENST00000448166.6:c.-103-36809A= (C1orf141)	ENSP00000415519.2:n.-103-36809A=
NM_144701.2:c.-29-56T= (IL23R)	NP_653302.2:n.-29-56T=
XM_011540789.1:c.62-56T= (IL23R)	XP_011539091.1:n.62-56T=
XM_011540790.1:c.-29-56T= (IL23R)	XP_011539092.1:n.-29-56T=
XM_011540791.1:c.-29-56T= (IL23R)	XP_011539093.1:n.-29-56T=
XM_011540790.3:c.-29-56T= (IL23R)	XP_011539092.1:n.-29-56T=
XM_011540791.3:c.-29-56T= (IL23R)	XP_011539093.1:n.-29-56T=
XR_001736993.1:n.155-56T= (IL23R)
NM_144701.3:c.-29-56T= (IL23R) MANE Select	NP_653302.2:n.-29-56T=