Canonical Allele Identifier: CA1173064248

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258735C= , CM000663.2:g.67258735C=	GRCh38
NC_000001.10:g.67724418C= , CM000663.1:g.67724418C=	GRCh37
NC_000001.9:g.67497006C=	NCBI36
NG_011498.1:g.97250C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1336C=	ENSP00000513138.1:n.1336C=
ENST00000697150.1:c.1394C=	ENSP00000513139.1:n.1394C=
ENST00000697151.1:c.1327C=	ENSP00000513140.1:n.1327C=
ENST00000697164.1:c.1407C=	ENSP00000513153.1:p.Ser469=
ENST00000697165.1:c.1194C=	ENSP00000513154.1:p.Ser398=
ENST00000347310.10:c.1497C= MANE Select	ENSP00000321345.5:p.Ser499=
ENST00000637002.1:c.888C=	ENSP00000490340.1:p.Ser296=
ENST00000347310.9:c.1497C=	ENSP00000321345.5:p.Ser499=
ENST00000395227.2:c.291C=	ENSP00000378652.2:p.Ser97=
ENST00000425614.3:c.732C=	ENSP00000387640.2:p.Ser244=
ENST00000473881.2:c.*323C=	ENSP00000486667.1:n.*323C=
NM_144701.2:c.1497C=	NP_653302.2:p.Ser499=
XM_005270516.2:c.735C=	XP_005270573.1:p.Ser245=
XM_011540789.1:c.1587C=	XP_011539091.1:p.Ser529=
XM_011540790.1:c.1497C=	XP_011539092.1:p.Ser499=
XM_011540791.1:c.1497C=	XP_011539093.1:p.Ser499=
XM_011540790.3:c.1497C=	XP_011539092.1:p.Ser499=
XM_011540791.3:c.1497C=	XP_011539093.1:p.Ser499=
XR_001736993.1:n.1577C=
NM_144701.3:c.1497C= MANE Select	NP_653302.2:p.Ser499=