Canonical Allele Identifier: CA1148877783

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258743A= , CM000663.2:g.67258743A=	GRCh38
NC_000001.10:g.67724426A= , CM000663.1:g.67724426A=	GRCh37
NC_000001.9:g.67497014A=	NCBI36
NG_011498.1:g.97258A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1344A=	ENSP00000513138.1:n.1344A=
ENST00000697150.1:c.1402A=	ENSP00000513139.1:n.1402A=
ENST00000697151.1:c.1335A=	ENSP00000513140.1:n.1335A=
ENST00000697164.1:c.1415A=	ENSP00000513153.1:p.Asn472=
ENST00000697165.1:c.1202A=	ENSP00000513154.1:p.Asn401=
ENST00000347310.10:c.1505A= MANE Select	ENSP00000321345.5:p.Asn502=
ENST00000637002.1:c.896A=	ENSP00000490340.1:p.Asn299=
ENST00000347310.9:c.1505A=	ENSP00000321345.5:p.Asn502=
ENST00000395227.2:c.299A=	ENSP00000378652.2:p.Asn100=
ENST00000425614.3:c.740A=	ENSP00000387640.2:p.Asn247=
ENST00000473881.2:c.*331A=	ENSP00000486667.1:n.*331A=
NM_144701.2:c.1505A=	NP_653302.2:p.Asn502=
XM_005270516.2:c.743A=	XP_005270573.1:p.Asn248=
XM_011540789.1:c.1595A=	XP_011539091.1:p.Asn532=
XM_011540790.1:c.1505A=	XP_011539092.1:p.Asn502=
XM_011540791.1:c.1505A=	XP_011539093.1:p.Asn502=
XM_011540790.3:c.1505A=	XP_011539092.1:p.Asn502=
XM_011540791.3:c.1505A=	XP_011539093.1:p.Asn502=
XR_001736993.1:n.1585A=
NM_144701.3:c.1505A= MANE Select	NP_653302.2:p.Asn502=