Canonical Allele Identifier: CA2574401473

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258909_67258910insC , CM000663.2:g.67258909_67258910insC	GRCh38
NC_000001.10:g.67724592_67724593insC , CM000663.1:g.67724592_67724593insC	GRCh37
NC_000001.9:g.67497180_67497181insC	NCBI36
NG_011498.1:g.97424_97425insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1510_1511insC	ENSP00000513138.1:n.1510_1511insC
ENST00000697150.1:c.1568_1569insC	ENSP00000513139.1:n.1568_1569insC
ENST00000697151.1:c.1501_1502insC	ENSP00000513140.1:n.1501_1502insC
ENST00000697164.1:c.1581_1582insC	ENSP00000513153.1:p.Cys528LeufsTer5
ENST00000697165.1:c.1368_1369insC	ENSP00000513154.1:p.Cys457LeufsTer5
ENST00000347310.10:c.1671_1672insC MANE Select	ENSP00000321345.5:p.Cys558LeufsTer5
ENST00000637002.1:c.1062_1063insC	ENSP00000490340.1:p.Cys355LeufsTer5
ENST00000347310.9:c.1671_1672insC	ENSP00000321345.5:p.Cys558LeufsTer5
ENST00000395227.2:c.465_466insC	ENSP00000378652.2:p.Cys156LeufsTer5
ENST00000425614.3:c.906_907insC	ENSP00000387640.2:p.Cys303LeufsTer5
ENST00000473881.2:c.*497_*498insC	ENSP00000486667.1:n.*497_*498insC
NM_144701.2:c.1671_1672insC	NP_653302.2:p.Cys558LeufsTer5
XM_005270516.2:c.909_910insC	XP_005270573.1:p.Cys304LeufsTer5
XM_011540789.1:c.1761_1762insC	XP_011539091.1:p.Cys588LeufsTer5
XM_011540790.1:c.1671_1672insC	XP_011539092.1:p.Cys558LeufsTer5
XM_011540791.1:c.1671_1672insC	XP_011539093.1:p.Cys558LeufsTer5
XM_011540790.3:c.1671_1672insC	XP_011539092.1:p.Cys558LeufsTer5
XM_011540791.3:c.1671_1672insC	XP_011539093.1:p.Cys558LeufsTer5
XR_001736993.1:n.1751_1752insC
NM_144701.3:c.1671_1672insC MANE Select	NP_653302.2:p.Cys558LeufsTer5