Canonical Allele Identifier: CA1173064297

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258921T= , CM000663.2:g.67258921T=	GRCh38
NC_000001.10:g.67724604T= , CM000663.1:g.67724604T=	GRCh37
NC_000001.9:g.67497192T=	NCBI36
NG_011498.1:g.97436T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1522T=	ENSP00000513138.1:n.1522T=
ENST00000697150.1:c.1580T=	ENSP00000513139.1:n.1580T=
ENST00000697151.1:c.1513T=	ENSP00000513140.1:n.1513T=
ENST00000697164.1:c.1593T=	ENSP00000513153.1:p.Pro531=
ENST00000697165.1:c.1380T=	ENSP00000513154.1:p.Pro460=
ENST00000347310.10:c.1683T= MANE Select	ENSP00000321345.5:p.Pro561=
ENST00000637002.1:c.1074T=	ENSP00000490340.1:p.Pro358=
ENST00000347310.9:c.1683T=	ENSP00000321345.5:p.Pro561=
ENST00000395227.2:c.477T=	ENSP00000378652.2:p.Pro159=
ENST00000425614.3:c.918T=	ENSP00000387640.2:p.Pro306=
ENST00000473881.2:c.*509T=	ENSP00000486667.1:n.*509T=
NM_144701.2:c.1683T=	NP_653302.2:p.Pro561=
XM_005270516.2:c.921T=	XP_005270573.1:p.Pro307=
XM_011540789.1:c.1773T=	XP_011539091.1:p.Pro591=
XM_011540790.1:c.1683T=	XP_011539092.1:p.Pro561=
XM_011540791.1:c.1683T=	XP_011539093.1:p.Pro561=
XM_011540790.3:c.1683T=	XP_011539092.1:p.Pro561=
XM_011540791.3:c.1683T=	XP_011539093.1:p.Pro561=
XR_001736993.1:n.1763T=
NM_144701.3:c.1683T= MANE Select	NP_653302.2:p.Pro561=