Canonical Allele Identifier: CA1173064295

Gene: IL23R

Linked Data

• dbSNP Id: rs1653097182

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258919_67258921del , CM000663.2:g.67258919_67258921del	GRCh38
NC_000001.10:g.67724602_67724604del , CM000663.1:g.67724602_67724604del	GRCh37
NC_000001.9:g.67497190_67497192del	NCBI36
NG_011498.1:g.97434_97436del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1520_1522del	ENSP00000513138.1:n.1520_1522del
ENST00000697150.1:c.1578_1580del	ENSP00000513139.1:n.1578_1580del
ENST00000697151.1:c.1511_1513del	ENSP00000513140.1:n.1511_1513del
ENST00000697164.1:c.1591_1593del	ENSP00000513153.1:p.Pro531del
ENST00000697165.1:c.1378_1380del	ENSP00000513154.1:p.Pro460del
ENST00000347310.10:c.1681_1683del MANE Select	ENSP00000321345.5:p.Pro561del
ENST00000637002.1:c.1072_1074del	ENSP00000490340.1:p.Pro358del
ENST00000347310.9:c.1681_1683del	ENSP00000321345.5:p.Pro561del
ENST00000395227.2:c.475_477del	ENSP00000378652.2:p.Pro159del
ENST00000425614.3:c.916_918del	ENSP00000387640.2:p.Pro306del
ENST00000473881.2:c.*507_*509del	ENSP00000486667.1:n.*507_*509del
NM_144701.2:c.1681_1683del	NP_653302.2:p.Pro561del
XM_005270516.2:c.919_921del	XP_005270573.1:p.Pro307del
XM_011540789.1:c.1771_1773del	XP_011539091.1:p.Pro591del
XM_011540790.1:c.1681_1683del	XP_011539092.1:p.Pro561del
XM_011540791.1:c.1681_1683del	XP_011539093.1:p.Pro561del
XM_011540790.3:c.1681_1683del	XP_011539092.1:p.Pro561del
XM_011540791.3:c.1681_1683del	XP_011539093.1:p.Pro561del
XR_001736993.1:n.1761_1763del
NM_144701.3:c.1681_1683del MANE Select	NP_653302.2:p.Pro561del