Canonical Allele Identifier: CA1142054296

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258843A= , CM000663.2:g.67258843A=	GRCh38
NC_000001.10:g.67724526A= , CM000663.1:g.67724526A=	GRCh37
NC_000001.9:g.67497114A=	NCBI36
NG_011498.1:g.97358A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1444A=	ENSP00000513138.1:n.1444A=
ENST00000697150.1:c.1502A=	ENSP00000513139.1:n.1502A=
ENST00000697151.1:c.1435A=	ENSP00000513140.1:n.1435A=
ENST00000697164.1:c.1515A=	ENSP00000513153.1:p.Ser505=
ENST00000697165.1:c.1302A=	ENSP00000513154.1:p.Ser434=
ENST00000347310.10:c.1605A= MANE Select	ENSP00000321345.5:p.Ser535=
ENST00000637002.1:c.996A=	ENSP00000490340.1:p.Ser332=
ENST00000347310.9:c.1605A=	ENSP00000321345.5:p.Ser535=
ENST00000395227.2:c.399A=	ENSP00000378652.2:p.Ser133=
ENST00000425614.3:c.840A=	ENSP00000387640.2:p.Ser280=
ENST00000473881.2:c.*431A=	ENSP00000486667.1:n.*431A=
NM_144701.2:c.1605A=	NP_653302.2:p.Ser535=
XM_005270516.2:c.843A=	XP_005270573.1:p.Ser281=
XM_011540789.1:c.1695A=	XP_011539091.1:p.Ser565=
XM_011540790.1:c.1605A=	XP_011539092.1:p.Ser535=
XM_011540791.1:c.1605A=	XP_011539093.1:p.Ser535=
XM_011540790.3:c.1605A=	XP_011539092.1:p.Ser535=
XM_011540791.3:c.1605A=	XP_011539093.1:p.Ser535=
XR_001736993.1:n.1685A=
NM_144701.3:c.1605A= MANE Select	NP_653302.2:p.Ser535=