Canonical Allele Identifier: CA1173064254

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258754T= , CM000663.2:g.67258754T=	GRCh38
NC_000001.10:g.67724437T= , CM000663.1:g.67724437T=	GRCh37
NC_000001.9:g.67497025T=	NCBI36
NG_011498.1:g.97269T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1355T=	ENSP00000513138.1:n.1355T=
ENST00000697150.1:c.1413T=	ENSP00000513139.1:n.1413T=
ENST00000697151.1:c.1346T=	ENSP00000513140.1:n.1346T=
ENST00000697164.1:c.1426T=	ENSP00000513153.1:p.Ser476=
ENST00000697165.1:c.1213T=	ENSP00000513154.1:p.Ser405=
ENST00000347310.10:c.1516T= MANE Select	ENSP00000321345.5:p.Ser506=
ENST00000637002.1:c.907T=	ENSP00000490340.1:p.Ser303=
ENST00000347310.9:c.1516T=	ENSP00000321345.5:p.Ser506=
ENST00000395227.2:c.310T=	ENSP00000378652.2:p.Ser104=
ENST00000425614.3:c.751T=	ENSP00000387640.2:p.Ser251=
ENST00000473881.2:c.*342T=	ENSP00000486667.1:n.*342T=
NM_144701.2:c.1516T=	NP_653302.2:p.Ser506=
XM_005270516.2:c.754T=	XP_005270573.1:p.Ser252=
XM_011540789.1:c.1606T=	XP_011539091.1:p.Ser536=
XM_011540790.1:c.1516T=	XP_011539092.1:p.Ser506=
XM_011540791.1:c.1516T=	XP_011539093.1:p.Ser506=
XM_011540790.3:c.1516T=	XP_011539092.1:p.Ser506=
XM_011540791.3:c.1516T=	XP_011539093.1:p.Ser506=
XR_001736993.1:n.1596T=
NM_144701.3:c.1516T= MANE Select	NP_653302.2:p.Ser506=