Canonical Allele Identifier: CA1173064263

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258785T= , CM000663.2:g.67258785T=	GRCh38
NC_000001.10:g.67724468T= , CM000663.1:g.67724468T=	GRCh37
NC_000001.9:g.67497056T=	NCBI36
NG_011498.1:g.97300T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1386T=	ENSP00000513138.1:n.1386T=
ENST00000697150.1:c.1444T=	ENSP00000513139.1:n.1444T=
ENST00000697151.1:c.1377T=	ENSP00000513140.1:n.1377T=
ENST00000697164.1:c.1457T=	ENSP00000513153.1:p.Leu486=
ENST00000697165.1:c.1244T=	ENSP00000513154.1:p.Leu415=
ENST00000347310.10:c.1547T= MANE Select	ENSP00000321345.5:p.Leu516=
ENST00000637002.1:c.938T=	ENSP00000490340.1:p.Leu313=
ENST00000347310.9:c.1547T=	ENSP00000321345.5:p.Leu516=
ENST00000395227.2:c.341T=	ENSP00000378652.2:p.Leu114=
ENST00000425614.3:c.782T=	ENSP00000387640.2:p.Leu261=
ENST00000473881.2:c.*373T=	ENSP00000486667.1:n.*373T=
NM_144701.2:c.1547T=	NP_653302.2:p.Leu516=
XM_005270516.2:c.785T=	XP_005270573.1:p.Leu262=
XM_011540789.1:c.1637T=	XP_011539091.1:p.Leu546=
XM_011540790.1:c.1547T=	XP_011539092.1:p.Leu516=
XM_011540791.1:c.1547T=	XP_011539093.1:p.Leu516=
XM_011540790.3:c.1547T=	XP_011539092.1:p.Leu516=
XM_011540791.3:c.1547T=	XP_011539093.1:p.Leu516=
XR_001736993.1:n.1627T=
NM_144701.3:c.1547T= MANE Select	NP_653302.2:p.Leu516=