Canonical Allele Identifier: CA1173064252

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258752C= , CM000663.2:g.67258752C=	GRCh38
NC_000001.10:g.67724435C= , CM000663.1:g.67724435C=	GRCh37
NC_000001.9:g.67497023C=	NCBI36
NG_011498.1:g.97267C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1353C=	ENSP00000513138.1:n.1353C=
ENST00000697150.1:c.1411C=	ENSP00000513139.1:n.1411C=
ENST00000697151.1:c.1344C=	ENSP00000513140.1:n.1344C=
ENST00000697164.1:c.1424C=	ENSP00000513153.1:p.Thr475=
ENST00000697165.1:c.1211C=	ENSP00000513154.1:p.Thr404=
ENST00000347310.10:c.1514C= MANE Select	ENSP00000321345.5:p.Thr505=
ENST00000637002.1:c.905C=	ENSP00000490340.1:p.Thr302=
ENST00000347310.9:c.1514C=	ENSP00000321345.5:p.Thr505=
ENST00000395227.2:c.308C=	ENSP00000378652.2:p.Thr103=
ENST00000425614.3:c.749C=	ENSP00000387640.2:p.Thr250=
ENST00000473881.2:c.*340C=	ENSP00000486667.1:n.*340C=
NM_144701.2:c.1514C=	NP_653302.2:p.Thr505=
XM_005270516.2:c.752C=	XP_005270573.1:p.Thr251=
XM_011540789.1:c.1604C=	XP_011539091.1:p.Thr535=
XM_011540790.1:c.1514C=	XP_011539092.1:p.Thr505=
XM_011540791.1:c.1514C=	XP_011539093.1:p.Thr505=
XM_011540790.3:c.1514C=	XP_011539092.1:p.Thr505=
XM_011540791.3:c.1514C=	XP_011539093.1:p.Thr505=
XR_001736993.1:n.1594C=
NM_144701.3:c.1514C= MANE Select	NP_653302.2:p.Thr505=