Canonical Allele Identifier: CA1173064271

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258827T= , CM000663.2:g.67258827T=	GRCh38
NC_000001.10:g.67724510T= , CM000663.1:g.67724510T=	GRCh37
NC_000001.9:g.67497098T=	NCBI36
NG_011498.1:g.97342T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1428T=	ENSP00000513138.1:n.1428T=
ENST00000697150.1:c.1486T=	ENSP00000513139.1:n.1486T=
ENST00000697151.1:c.1419T=	ENSP00000513140.1:n.1419T=
ENST00000697164.1:c.1499T=	ENSP00000513153.1:p.Phe500=
ENST00000697165.1:c.1286T=	ENSP00000513154.1:p.Phe429=
ENST00000347310.10:c.1589T= MANE Select	ENSP00000321345.5:p.Phe530=
ENST00000637002.1:c.980T=	ENSP00000490340.1:p.Phe327=
ENST00000347310.9:c.1589T=	ENSP00000321345.5:p.Phe530=
ENST00000395227.2:c.383T=	ENSP00000378652.2:p.Phe128=
ENST00000425614.3:c.824T=	ENSP00000387640.2:p.Phe275=
ENST00000473881.2:c.*415T=	ENSP00000486667.1:n.*415T=
NM_144701.2:c.1589T=	NP_653302.2:p.Phe530=
XM_005270516.2:c.827T=	XP_005270573.1:p.Phe276=
XM_011540789.1:c.1679T=	XP_011539091.1:p.Phe560=
XM_011540790.1:c.1589T=	XP_011539092.1:p.Phe530=
XM_011540791.1:c.1589T=	XP_011539093.1:p.Phe530=
XM_011540790.3:c.1589T=	XP_011539092.1:p.Phe530=
XM_011540791.3:c.1589T=	XP_011539093.1:p.Phe530=
XR_001736993.1:n.1669T=
NM_144701.3:c.1589T= MANE Select	NP_653302.2:p.Phe530=