Canonical Allele Identifier: CA1173064274

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258841T= , CM000663.2:g.67258841T=	GRCh38
NC_000001.10:g.67724524T= , CM000663.1:g.67724524T=	GRCh37
NC_000001.9:g.67497112T=	NCBI36
NG_011498.1:g.97356T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1442T=	ENSP00000513138.1:n.1442T=
ENST00000697150.1:c.1500T=	ENSP00000513139.1:n.1500T=
ENST00000697151.1:c.1433T=	ENSP00000513140.1:n.1433T=
ENST00000697164.1:c.1513T=	ENSP00000513153.1:p.Ser505=
ENST00000697165.1:c.1300T=	ENSP00000513154.1:p.Ser434=
ENST00000347310.10:c.1603T= MANE Select	ENSP00000321345.5:p.Ser535=
ENST00000637002.1:c.994T=	ENSP00000490340.1:p.Ser332=
ENST00000347310.9:c.1603T=	ENSP00000321345.5:p.Ser535=
ENST00000395227.2:c.397T=	ENSP00000378652.2:p.Ser133=
ENST00000425614.3:c.838T=	ENSP00000387640.2:p.Ser280=
ENST00000473881.2:c.*429T=	ENSP00000486667.1:n.*429T=
NM_144701.2:c.1603T=	NP_653302.2:p.Ser535=
XM_005270516.2:c.841T=	XP_005270573.1:p.Ser281=
XM_011540789.1:c.1693T=	XP_011539091.1:p.Ser565=
XM_011540790.1:c.1603T=	XP_011539092.1:p.Ser535=
XM_011540791.1:c.1603T=	XP_011539093.1:p.Ser535=
XM_011540790.3:c.1603T=	XP_011539092.1:p.Ser535=
XM_011540791.3:c.1603T=	XP_011539093.1:p.Ser535=
XR_001736993.1:n.1683T=
NM_144701.3:c.1603T= MANE Select	NP_653302.2:p.Ser535=