Canonical Allele Identifier: CA1173064259

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258770C= , CM000663.2:g.67258770C=	GRCh38
NC_000001.10:g.67724453C= , CM000663.1:g.67724453C=	GRCh37
NC_000001.9:g.67497041C=	NCBI36
NG_011498.1:g.97285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1371C=	ENSP00000513138.1:n.1371C=
ENST00000697150.1:c.1429C=	ENSP00000513139.1:n.1429C=
ENST00000697151.1:c.1362C=	ENSP00000513140.1:n.1362C=
ENST00000697164.1:c.1442C=	ENSP00000513153.1:p.Pro481=
ENST00000697165.1:c.1229C=	ENSP00000513154.1:p.Pro410=
ENST00000347310.10:c.1532C= MANE Select	ENSP00000321345.5:p.Pro511=
ENST00000637002.1:c.923C=	ENSP00000490340.1:p.Pro308=
ENST00000347310.9:c.1532C=	ENSP00000321345.5:p.Pro511=
ENST00000395227.2:c.326C=	ENSP00000378652.2:p.Pro109=
ENST00000425614.3:c.767C=	ENSP00000387640.2:p.Pro256=
ENST00000473881.2:c.*358C=	ENSP00000486667.1:n.*358C=
NM_144701.2:c.1532C=	NP_653302.2:p.Pro511=
XM_005270516.2:c.770C=	XP_005270573.1:p.Pro257=
XM_011540789.1:c.1622C=	XP_011539091.1:p.Pro541=
XM_011540790.1:c.1532C=	XP_011539092.1:p.Pro511=
XM_011540791.1:c.1532C=	XP_011539093.1:p.Pro511=
XM_011540790.3:c.1532C=	XP_011539092.1:p.Pro511=
XM_011540791.3:c.1532C=	XP_011539093.1:p.Pro511=
XR_001736993.1:n.1612C=
NM_144701.3:c.1532C= MANE Select	NP_653302.2:p.Pro511=