Canonical Allele Identifier: CA1173064314

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258983A= , CM000663.2:g.67258983A=	GRCh38
NC_000001.10:g.67724666A= , CM000663.1:g.67724666A=	GRCh37
NC_000001.9:g.67497254A=	NCBI36
NG_011498.1:g.97498A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1584A=	ENSP00000513138.1:n.1584A=
ENST00000697150.1:c.1642A=	ENSP00000513139.1:n.1642A=
ENST00000697151.1:c.1575A=	ENSP00000513140.1:n.1575A=
ENST00000697164.1:c.1655A=	ENSP00000513153.1:p.Glu552=
ENST00000697165.1:c.1442A=	ENSP00000513154.1:p.Glu481=
ENST00000347310.10:c.1745A= MANE Select	ENSP00000321345.5:p.Glu582=
ENST00000637002.1:c.1136A=	ENSP00000490340.1:p.Glu379=
ENST00000347310.9:c.1745A=	ENSP00000321345.5:p.Glu582=
ENST00000395227.2:c.539A=	ENSP00000378652.2:p.Glu180=
ENST00000425614.3:c.980A=	ENSP00000387640.2:p.Glu327=
ENST00000473881.2:c.*571A=	ENSP00000486667.1:n.*571A=
NM_144701.2:c.1745A=	NP_653302.2:p.Glu582=
XM_005270516.2:c.983A=	XP_005270573.1:p.Glu328=
XM_011540789.1:c.1835A=	XP_011539091.1:p.Glu612=
XM_011540790.1:c.1745A=	XP_011539092.1:p.Glu582=
XM_011540791.1:c.1745A=	XP_011539093.1:p.Glu582=
XM_011540790.3:c.1745A=	XP_011539092.1:p.Glu582=
XM_011540791.3:c.1745A=	XP_011539093.1:p.Glu582=
XR_001736993.1:n.1825A=
NM_144701.3:c.1745A= MANE Select	NP_653302.2:p.Glu582=