Canonical Allele Identifier: CA2573132499

Gene: IL23R

Linked Data

• ClinVar Variation Id: 1517093
• ClinVar RCV Id: RCV002041005
• dbSNP Id: rs2100398583

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258972_67258975dup , CM000663.2:g.67258972_67258975dup	GRCh38
NC_000001.10:g.67724655_67724658dup , CM000663.1:g.67724655_67724658dup	GRCh37
NC_000001.9:g.67497243_67497246dup	NCBI36
NG_011498.1:g.97487_97490dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1573_1576dup	ENSP00000513138.1:n.1573_1576dup
ENST00000697150.1:c.1631_1634dup	ENSP00000513139.1:n.1631_1634dup
ENST00000697151.1:c.1564_1567dup	ENSP00000513140.1:n.1564_1567dup
ENST00000697164.1:c.1644_1647dup	ENSP00000513153.1:p.Pro550PhefsTer4
ENST00000697165.1:c.1431_1434dup	ENSP00000513154.1:p.Pro479PhefsTer4
ENST00000347310.10:c.1734_1737dup MANE Select	ENSP00000321345.5:p.Pro580PhefsTer4
ENST00000637002.1:c.1125_1128dup	ENSP00000490340.1:p.Pro377PhefsTer4
ENST00000347310.9:c.1734_1737dup	ENSP00000321345.5:p.Pro580PhefsTer4
ENST00000395227.2:c.528_531dup	ENSP00000378652.2:p.Pro178PhefsTer4
ENST00000425614.3:c.969_972dup	ENSP00000387640.2:p.Pro325PhefsTer4
ENST00000473881.2:c.*560_*563dup	ENSP00000486667.1:n.*560_*563dup
NM_144701.2:c.1734_1737dup	NP_653302.2:p.Pro580PhefsTer4
XM_005270516.2:c.972_975dup	XP_005270573.1:p.Pro326PhefsTer4
XM_011540789.1:c.1824_1827dup	XP_011539091.1:p.Pro610PhefsTer4
XM_011540790.1:c.1734_1737dup	XP_011539092.1:p.Pro580PhefsTer4
XM_011540791.1:c.1734_1737dup	XP_011539093.1:p.Pro580PhefsTer4
XM_011540790.3:c.1734_1737dup	XP_011539092.1:p.Pro580PhefsTer4
XM_011540791.3:c.1734_1737dup	XP_011539093.1:p.Pro580PhefsTer4
XR_001736993.1:n.1814_1817dup
NM_144701.3:c.1734_1737dup MANE Select	NP_653302.2:p.Pro580PhefsTer4