Canonical Allele Identifier: CA1173064338

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259060A= , CM000663.2:g.67259060A=	GRCh38
NC_000001.10:g.67724743A= , CM000663.1:g.67724743A=	GRCh37
NC_000001.9:g.67497331A=	NCBI36
NG_011498.1:g.97575A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1661A=	ENSP00000513138.1:n.1661A=
ENST00000697150.1:c.1719A=	ENSP00000513139.1:n.1719A=
ENST00000697151.1:c.1652A=	ENSP00000513140.1:n.1652A=
ENST00000697164.1:c.1732A=	ENSP00000513153.1:p.Ile578=
ENST00000697165.1:c.1519A=	ENSP00000513154.1:p.Ile507=
ENST00000347310.10:c.1822A= MANE Select	ENSP00000321345.5:p.Ile608=
ENST00000637002.1:c.1213A=	ENSP00000490340.1:p.Ile405=
ENST00000347310.9:c.1822A=	ENSP00000321345.5:p.Ile608=
ENST00000395227.2:c.616A=	ENSP00000378652.2:p.Ile206=
ENST00000425614.3:c.1057A=	ENSP00000387640.2:p.Ile353=
ENST00000473881.2:c.*648A=	ENSP00000486667.1:n.*648A=
NM_144701.2:c.1822A=	NP_653302.2:p.Ile608=
XM_005270516.2:c.1060A=	XP_005270573.1:p.Ile354=
XM_011540789.1:c.1912A=	XP_011539091.1:p.Ile638=
XM_011540790.1:c.1822A=	XP_011539092.1:p.Ile608=
XM_011540791.1:c.1822A=	XP_011539093.1:p.Ile608=
XM_011540790.3:c.1822A=	XP_011539092.1:p.Ile608=
XM_011540791.3:c.1822A=	XP_011539093.1:p.Ile608=
XR_001736993.1:n.1902A=
NM_144701.3:c.1822A= MANE Select	NP_653302.2:p.Ile608=