Canonical Allele Identifier: CA1002752924

Gene: IL23R

Linked Data

• gnomAD v3: 1-67255447-A-ATTTT
• gnomAD v4: 1-67255447-A-ATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67255454_67255457dup , CM000663.2:g.67255454_67255457dup	GRCh38
NC_000001.10:g.67721137_67721140dup , CM000663.1:g.67721137_67721140dup	GRCh37
NC_000001.9:g.67493725_67493728dup	NCBI36
NG_011498.1:g.93969_93972dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000697148.1:c.1025-383_1025-380dup	ENSP00000513137.1:n.1025-383_1025-380dup
ENST00000697149.1:c.988-383_988-380dup	ENSP00000513138.1:n.988-383_988-380dup
ENST00000697150.1:c.1046-383_1046-380dup	ENSP00000513139.1:n.1046-383_1046-380dup
ENST00000697151.1:c.1046-383_1046-380dup	ENSP00000513140.1:n.1046-383_1046-380dup
ENST00000697152.1:c.799-383_799-380dup	ENSP00000513141.1:n.799-383_799-380dup
ENST00000697153.1:c.795-383_795-380dup	ENSP00000513142.1:n.795-383_795-380dup
ENST00000697154.1:c.956-3024_956-3021dup	ENSP00000513143.1:n.956-3024_956-3021dup
ENST00000697155.1:c.649-3024_649-3021dup	ENSP00000513144.1:n.649-3024_649-3021dup
ENST00000697156.1:c.1282-383_1282-380dup	ENSP00000513145.1:n.1282-383_1282-380dup
ENST00000697157.1:c.1003-383_1003-380dup	ENSP00000513146.1:n.1003-383_1003-380dup
ENST00000697158.1:c.992-383_992-380dup	ENSP00000513147.1:n.992-383_992-380dup
ENST00000697159.1:c.842-383_842-380dup	ENSP00000513148.1:n.842-383_842-380dup
ENST00000697160.1:c.956-383_956-380dup	ENSP00000513149.1:n.956-383_956-380dup
ENST00000697161.1:c.685-383_685-380dup	ENSP00000513150.1:n.685-383_685-380dup
ENST00000697162.1:c.1078-383_1078-380dup	ENSP00000513151.1:n.1078-383_1078-380dup
ENST00000697163.1:c.1149-383_1149-380dup	ENSP00000513152.1:n.1149-383_1149-380dup
ENST00000697164.1:c.1059-383_1059-380dup	ENSP00000513153.1:n.1059-383_1059-380dup
ENST00000697165.1:c.846-383_846-380dup	ENSP00000513154.1:n.846-383_846-380dup
ENST00000697223.1:c.898-383_898-380dup	ENSP00000513190.1:n.898-383_898-380dup
ENST00000697224.1:c.885-383_885-380dup	ENSP00000513191.1:n.885-383_885-380dup
ENST00000697225.1:c.752-383_752-380dup	ENSP00000513192.1:n.752-383_752-380dup
ENST00000697226.1:c.739-383_739-380dup	ENSP00000513193.1:n.739-383_739-380dup
ENST00000697227.1:c.985-383_985-380dup	ENSP00000513194.1:n.985-383_985-380dup
ENST00000697228.1:c.841-383_841-380dup	ENSP00000513195.1:n.841-383_841-380dup
ENST00000697229.1:c.885-383_885-380dup	ENSP00000513196.1:n.885-383_885-380dup
ENST00000697230.1:c.1059-383_1059-380dup	ENSP00000513197.1:n.1059-383_1059-380dup
ENST00000697231.1:c.1054-383_1054-380dup	ENSP00000513198.1:n.1054-383_1054-380dup
ENST00000697232.1:c.1240-383_1240-380dup	ENSP00000513199.1:n.1240-383_1240-380dup
ENST00000347310.10:c.1149-383_1149-380dup MANE Select	ENSP00000321345.5:n.1149-383_1149-380dup
ENST00000637002.1:c.540-383_540-380dup	ENSP00000490340.1:n.540-383_540-380dup
ENST00000347310.9:c.1149-383_1149-380dup	ENSP00000321345.5:n.1149-383_1149-380dup
ENST00000395227.2:c.-58-383_-58-380dup	ENSP00000378652.2:n.-58-383_-58-380dup
ENST00000425614.3:c.384-383_384-380dup	ENSP00000387640.2:n.384-383_384-380dup
ENST00000473881.2:c.191-383_191-380dup	ENSP00000486667.1:n.191-383_191-380dup
NM_144701.2:c.1149-383_1149-380dup	NP_653302.2:n.1149-383_1149-380dup
XM_005270516.2:c.387-383_387-380dup	XP_005270573.1:n.387-383_387-380dup
XM_011540789.1:c.1239-383_1239-380dup	XP_011539091.1:n.1239-383_1239-380dup
XM_011540790.1:c.1149-383_1149-380dup	XP_011539092.1:n.1149-383_1149-380dup
XM_011540791.1:c.1149-383_1149-380dup	XP_011539093.1:n.1149-383_1149-380dup
XM_011540790.3:c.1149-383_1149-380dup	XP_011539092.1:n.1149-383_1149-380dup
XM_011540791.3:c.1149-383_1149-380dup	XP_011539093.1:n.1149-383_1149-380dup
XR_001736993.1:n.1229-383_1229-380dup
NM_144701.3:c.1149-383_1149-380dup MANE Select	NP_653302.2:n.1149-383_1149-380dup