Canonical Allele Identifier: CA1173056536

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240192C= , CM000663.2:g.67240192C=	GRCh38
NC_000001.10:g.67705875C= , CM000663.1:g.67705875C=	GRCh37
NC_000001.9:g.67478463C=	NCBI36
NG_011498.1:g.78707C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.935C=	ENSP00000513137.1:n.935C=
ENST00000697149.1:c.898C=	ENSP00000513138.1:n.898C=
ENST00000697150.1:c.1045+3390C=	ENSP00000513139.1:n.1045+3390C=
ENST00000697151.1:c.1045+3390C=	ENSP00000513140.1:n.1045+3390C=
ENST00000697152.1:c.799-15645C=	ENSP00000513141.1:n.799-15645C=
ENST00000697153.1:c.795-15645C=	ENSP00000513142.1:n.795-15645C=
ENST00000697154.1:c.956-18286C=	ENSP00000513143.1:n.956-18286C=
ENST00000697155.1:c.649-18286C=	ENSP00000513144.1:n.649-18286C=
ENST00000697156.1:c.1059C=	ENSP00000513145.1:p.Asp353=
ENST00000697157.1:c.913C=	ENSP00000513146.1:n.913C=
ENST00000697158.1:c.902C=	ENSP00000513147.1:n.902C=
ENST00000697159.1:c.752C=	ENSP00000513148.1:n.752C=
ENST00000697160.1:c.956-15645C=	ENSP00000513149.1:n.956-15645C=
ENST00000697161.1:c.595C=	ENSP00000513150.1:n.595C=
ENST00000697162.1:c.988C=	ENSP00000513151.1:n.988C=
ENST00000697163.1:c.1059C=	ENSP00000513152.1:p.Asp353=
ENST00000697164.1:c.969C=	ENSP00000513153.1:p.Asp323=
ENST00000697165.1:c.756C=	ENSP00000513154.1:p.Asp252=
ENST00000697223.1:c.808C=	ENSP00000513190.1:n.808C=
ENST00000697224.1:c.884+3390C=	ENSP00000513191.1:n.884+3390C=
ENST00000697225.1:c.662C=	ENSP00000513192.1:n.662C=
ENST00000697226.1:c.738+3390C=	ENSP00000513193.1:n.738+3390C=
ENST00000697227.1:c.895C=	ENSP00000513194.1:n.895C=
ENST00000697228.1:c.751C=	ENSP00000513195.1:n.751C=
ENST00000697229.1:c.885-15645C=	ENSP00000513196.1:n.885-15645C=
ENST00000697230.1:c.969C=	ENSP00000513197.1:p.Asp323=
ENST00000697231.1:c.964C=	ENSP00000513198.1:n.964C=
ENST00000697232.1:c.988C=	ENSP00000513199.1:n.988C=
ENST00000347310.10:c.1059C= MANE Select	ENSP00000321345.5:p.Asp353=
ENST00000637002.1:c.450C=	ENSP00000490340.1:p.Asp150=
ENST00000347310.9:c.1059C=	ENSP00000321345.5:p.Asp353=
ENST00000395227.2:c.-58-15645C=	ENSP00000378652.2:n.-58-15645C=
ENST00000425614.3:c.294C=	ENSP00000387640.2:p.Asp98=
ENST00000473881.2:c.191-15645C=	ENSP00000486667.1:n.191-15645C=
NM_144701.2:c.1059C=	NP_653302.2:p.Asp353=
XM_005270516.2:c.297C=	XP_005270573.1:p.Asp99=
XM_011540789.1:c.1149C=	XP_011539091.1:p.Asp383=
XM_011540790.1:c.1059C=	XP_011539092.1:p.Asp353=
XM_011540791.1:c.1059C=	XP_011539093.1:p.Asp353=
XM_011540790.3:c.1059C=	XP_011539092.1:p.Asp353=
XM_011540791.3:c.1059C=	XP_011539093.1:p.Asp353=
XR_001736993.1:n.1228+3390C=
NM_144701.3:c.1059C= MANE Select	NP_653302.2:p.Asp353=