Canonical Allele Identifier: CA1173064249

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258737A= , CM000663.2:g.67258737A=	GRCh38
NC_000001.10:g.67724420A= , CM000663.1:g.67724420A=	GRCh37
NC_000001.9:g.67497008A=	NCBI36
NG_011498.1:g.97252A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1338A=	ENSP00000513138.1:n.1338A=
ENST00000697150.1:c.1396A=	ENSP00000513139.1:n.1396A=
ENST00000697151.1:c.1329A=	ENSP00000513140.1:n.1329A=
ENST00000697164.1:c.1409A=	ENSP00000513153.1:p.Asn470=
ENST00000697165.1:c.1196A=	ENSP00000513154.1:p.Asn399=
ENST00000347310.10:c.1499A= MANE Select	ENSP00000321345.5:p.Asn500=
ENST00000637002.1:c.890A=	ENSP00000490340.1:p.Asn297=
ENST00000347310.9:c.1499A=	ENSP00000321345.5:p.Asn500=
ENST00000395227.2:c.293A=	ENSP00000378652.2:p.Asn98=
ENST00000425614.3:c.734A=	ENSP00000387640.2:p.Asn245=
ENST00000473881.2:c.*325A=	ENSP00000486667.1:n.*325A=
NM_144701.2:c.1499A=	NP_653302.2:p.Asn500=
XM_005270516.2:c.737A=	XP_005270573.1:p.Asn246=
XM_011540789.1:c.1589A=	XP_011539091.1:p.Asn530=
XM_011540790.1:c.1499A=	XP_011539092.1:p.Asn500=
XM_011540791.1:c.1499A=	XP_011539093.1:p.Asn500=
XM_011540790.3:c.1499A=	XP_011539092.1:p.Asn500=
XM_011540791.3:c.1499A=	XP_011539093.1:p.Asn500=
XR_001736993.1:n.1579A=
NM_144701.3:c.1499A= MANE Select	NP_653302.2:p.Asn500=