Canonical Allele Identifier: CA2646125616

Gene: IL23R

Linked Data

• gnomAD v4: 1-67240219-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240222dup , CM000663.2:g.67240222dup	GRCh38
NC_000001.10:g.67705905dup , CM000663.1:g.67705905dup	GRCh37
NC_000001.9:g.67478493dup	NCBI36
NG_011498.1:g.78737dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.965dup	ENSP00000513137.1:n.965dup
ENST00000697149.1:c.928dup	ENSP00000513138.1:n.928dup
ENST00000697150.1:c.1045+3420dup	ENSP00000513139.1:n.1045+3420dup
ENST00000697151.1:c.1045+3420dup	ENSP00000513140.1:n.1045+3420dup
ENST00000697152.1:c.799-15615dup	ENSP00000513141.1:n.799-15615dup
ENST00000697153.1:c.795-15615dup	ENSP00000513142.1:n.795-15615dup
ENST00000697154.1:c.956-18256dup	ENSP00000513143.1:n.956-18256dup
ENST00000697155.1:c.649-18256dup	ENSP00000513144.1:n.649-18256dup
ENST00000697156.1:c.1089dup	ENSP00000513145.1:p.Ala364CysfsTer14
ENST00000697157.1:c.943dup	ENSP00000513146.1:n.943dup
ENST00000697158.1:c.932dup	ENSP00000513147.1:n.932dup
ENST00000697159.1:c.782dup	ENSP00000513148.1:n.782dup
ENST00000697160.1:c.956-15615dup	ENSP00000513149.1:n.956-15615dup
ENST00000697161.1:c.625dup	ENSP00000513150.1:n.625dup
ENST00000697162.1:c.1018dup	ENSP00000513151.1:n.1018dup
ENST00000697163.1:c.1089dup	ENSP00000513152.1:p.Ala364CysfsTer14
ENST00000697164.1:c.999dup	ENSP00000513153.1:p.Ala334CysfsTer14
ENST00000697165.1:c.786dup	ENSP00000513154.1:p.Ala263CysfsTer14
ENST00000697223.1:c.838dup	ENSP00000513190.1:n.838dup
ENST00000697224.1:c.884+3420dup	ENSP00000513191.1:n.884+3420dup
ENST00000697225.1:c.692dup	ENSP00000513192.1:n.692dup
ENST00000697226.1:c.738+3420dup	ENSP00000513193.1:n.738+3420dup
ENST00000697227.1:c.925dup	ENSP00000513194.1:n.925dup
ENST00000697228.1:c.781dup	ENSP00000513195.1:n.781dup
ENST00000697229.1:c.885-15615dup	ENSP00000513196.1:n.885-15615dup
ENST00000697230.1:c.999dup	ENSP00000513197.1:p.Ala334CysfsTer14
ENST00000697231.1:c.994dup	ENSP00000513198.1:n.994dup
ENST00000697232.1:c.1018dup	ENSP00000513199.1:n.1018dup
ENST00000347310.10:c.1089dup MANE Select	ENSP00000321345.5:p.Ala364CysfsTer14
ENST00000637002.1:c.480dup	ENSP00000490340.1:p.Ala161CysfsTer14
ENST00000347310.9:c.1089dup	ENSP00000321345.5:p.Ala364CysfsTer14
ENST00000395227.2:c.-58-15615dup	ENSP00000378652.2:n.-58-15615dup
ENST00000425614.3:c.324dup	ENSP00000387640.2:p.Ala109CysfsTer14
ENST00000473881.2:c.191-15615dup	ENSP00000486667.1:n.191-15615dup
NM_144701.2:c.1089dup	NP_653302.2:p.Ala364CysfsTer14
XM_005270516.2:c.327dup	XP_005270573.1:p.Ala110CysfsTer14
XM_011540789.1:c.1179dup	XP_011539091.1:p.Ala394CysfsTer14
XM_011540790.1:c.1089dup	XP_011539092.1:p.Ala364CysfsTer14
XM_011540791.1:c.1089dup	XP_011539093.1:p.Ala364CysfsTer14
XM_011540790.3:c.1089dup	XP_011539092.1:p.Ala364CysfsTer14
XM_011540791.3:c.1089dup	XP_011539093.1:p.Ala364CysfsTer14
XR_001736993.1:n.1228+3420dup
NM_144701.3:c.1089dup MANE Select	NP_653302.2:p.Ala364CysfsTer14