Canonical Allele Identifier: CA2646125921

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258901-CAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258902_67258904del , CM000663.2:g.67258902_67258904del	GRCh38
NC_000001.10:g.67724585_67724587del , CM000663.1:g.67724585_67724587del	GRCh37
NC_000001.9:g.67497173_67497175del	NCBI36
NG_011498.1:g.97417_97419del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1503_1505del	ENSP00000513138.1:n.1503_1505del
ENST00000697150.1:c.1561_1563del	ENSP00000513139.1:n.1561_1563del
ENST00000697151.1:c.1494_1496del	ENSP00000513140.1:n.1494_1496del
ENST00000697164.1:c.1574_1576del	ENSP00000513153.1:p.Gln525_Gly526delinsArg
ENST00000697165.1:c.1361_1363del	ENSP00000513154.1:p.Gln454_Gly455delinsArg
ENST00000347310.10:c.1664_1666del MANE Select	ENSP00000321345.5:p.Gln555_Gly556delinsArg
ENST00000637002.1:c.1055_1057del	ENSP00000490340.1:p.Gln352_Gly353delinsArg
ENST00000347310.9:c.1664_1666del	ENSP00000321345.5:p.Gln555_Gly556delinsArg
ENST00000395227.2:c.458_460del	ENSP00000378652.2:p.Gln153_Gly154delinsArg
ENST00000425614.3:c.899_901del	ENSP00000387640.2:p.Gln300_Gly301delinsArg
ENST00000473881.2:c.*490_*492del	ENSP00000486667.1:n.*490_*492del
NM_144701.2:c.1664_1666del	NP_653302.2:p.Gln555_Gly556delinsArg
XM_005270516.2:c.902_904del	XP_005270573.1:p.Gln301_Gly302delinsArg
XM_011540789.1:c.1754_1756del	XP_011539091.1:p.Gln585_Gly586delinsArg
XM_011540790.1:c.1664_1666del	XP_011539092.1:p.Gln555_Gly556delinsArg
XM_011540791.1:c.1664_1666del	XP_011539093.1:p.Gln555_Gly556delinsArg
XM_011540790.3:c.1664_1666del	XP_011539092.1:p.Gln555_Gly556delinsArg
XM_011540791.3:c.1664_1666del	XP_011539093.1:p.Gln555_Gly556delinsArg
XR_001736993.1:n.1744_1746del
NM_144701.3:c.1664_1666del MANE Select	NP_653302.2:p.Gln555_Gly556delinsArg