Canonical Allele Identifier: CA1173064317

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258987T= , CM000663.2:g.67258987T=	GRCh38
NC_000001.10:g.67724670T= , CM000663.1:g.67724670T=	GRCh37
NC_000001.9:g.67497258T=	NCBI36
NG_011498.1:g.97502T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1588T=	ENSP00000513138.1:n.1588T=
ENST00000697150.1:c.1646T=	ENSP00000513139.1:n.1646T=
ENST00000697151.1:c.1579T=	ENSP00000513140.1:n.1579T=
ENST00000697164.1:c.1659T=	ENSP00000513153.1:p.Thr553=
ENST00000697165.1:c.1446T=	ENSP00000513154.1:p.Thr482=
ENST00000347310.10:c.1749T= MANE Select	ENSP00000321345.5:p.Thr583=
ENST00000637002.1:c.1140T=	ENSP00000490340.1:p.Thr380=
ENST00000347310.9:c.1749T=	ENSP00000321345.5:p.Thr583=
ENST00000395227.2:c.543T=	ENSP00000378652.2:p.Thr181=
ENST00000425614.3:c.984T=	ENSP00000387640.2:p.Thr328=
ENST00000473881.2:c.*575T=	ENSP00000486667.1:n.*575T=
NM_144701.2:c.1749T=	NP_653302.2:p.Thr583=
XM_005270516.2:c.987T=	XP_005270573.1:p.Thr329=
XM_011540789.1:c.1839T=	XP_011539091.1:p.Thr613=
XM_011540790.1:c.1749T=	XP_011539092.1:p.Thr583=
XM_011540791.1:c.1749T=	XP_011539093.1:p.Thr583=
XM_011540790.3:c.1749T=	XP_011539092.1:p.Thr583=
XM_011540791.3:c.1749T=	XP_011539093.1:p.Thr583=
XR_001736993.1:n.1829T=
NM_144701.3:c.1749T= MANE Select	NP_653302.2:p.Thr583=