Canonical Allele Identifier: CA1173064298

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258924C= , CM000663.2:g.67258924C=	GRCh38
NC_000001.10:g.67724607C= , CM000663.1:g.67724607C=	GRCh37
NC_000001.9:g.67497195C=	NCBI36
NG_011498.1:g.97439C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1525C=	ENSP00000513138.1:n.1525C=
ENST00000697150.1:c.1583C=	ENSP00000513139.1:n.1583C=
ENST00000697151.1:c.1516C=	ENSP00000513140.1:n.1516C=
ENST00000697164.1:c.1596C=	ENSP00000513153.1:p.Asp532=
ENST00000697165.1:c.1383C=	ENSP00000513154.1:p.Asp461=
ENST00000347310.10:c.1686C= MANE Select	ENSP00000321345.5:p.Asp562=
ENST00000637002.1:c.1077C=	ENSP00000490340.1:p.Asp359=
ENST00000347310.9:c.1686C=	ENSP00000321345.5:p.Asp562=
ENST00000395227.2:c.480C=	ENSP00000378652.2:p.Asp160=
ENST00000425614.3:c.921C=	ENSP00000387640.2:p.Asp307=
ENST00000473881.2:c.*512C=	ENSP00000486667.1:n.*512C=
NM_144701.2:c.1686C=	NP_653302.2:p.Asp562=
XM_005270516.2:c.924C=	XP_005270573.1:p.Asp308=
XM_011540789.1:c.1776C=	XP_011539091.1:p.Asp592=
XM_011540790.1:c.1686C=	XP_011539092.1:p.Asp562=
XM_011540791.1:c.1686C=	XP_011539093.1:p.Asp562=
XM_011540790.3:c.1686C=	XP_011539092.1:p.Asp562=
XM_011540791.3:c.1686C=	XP_011539093.1:p.Asp562=
XR_001736993.1:n.1766C=
NM_144701.3:c.1686C= MANE Select	NP_653302.2:p.Asp562=