Canonical Allele Identifier: CA340725875

Gene: IL23R

Linked Data

• COSMIC: COSM911826
• MyVariant Identifiers: chr1:g.67705928C>A (hg19) ; chr1:g.67240245C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67240245C>A , CM000663.2:g.67240245C>A	GRCh38
NC_000001.10:g.67705928C>A , CM000663.1:g.67705928C>A	GRCh37
NC_000001.9:g.67478516C>A	NCBI36
NG_011498.1:g.78760C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.988C>A	ENSP00000513137.1:n.988C>A
ENST00000697149.1:c.951C>A	ENSP00000513138.1:n.951C>A
ENST00000697150.1:c.1045+3443C>A	ENSP00000513139.1:n.1045+3443C>A
ENST00000697151.1:c.1045+3443C>A	ENSP00000513140.1:n.1045+3443C>A
ENST00000697152.1:c.799-15592C>A	ENSP00000513141.1:n.799-15592C>A
ENST00000697153.1:c.795-15592C>A	ENSP00000513142.1:n.795-15592C>A
ENST00000697154.1:c.956-18233C>A	ENSP00000513143.1:n.956-18233C>A
ENST00000697155.1:c.649-18233C>A	ENSP00000513144.1:n.649-18233C>A
ENST00000697156.1:c.1112C>A	ENSP00000513145.1:p.Ser371Tyr
ENST00000697157.1:c.966C>A	ENSP00000513146.1:n.966C>A
ENST00000697158.1:c.955C>A	ENSP00000513147.1:n.955C>A
ENST00000697159.1:c.805C>A	ENSP00000513148.1:n.805C>A
ENST00000697160.1:c.956-15592C>A	ENSP00000513149.1:n.956-15592C>A
ENST00000697161.1:c.648C>A	ENSP00000513150.1:n.648C>A
ENST00000697162.1:c.1041C>A	ENSP00000513151.1:n.1041C>A
ENST00000697163.1:c.1112C>A	ENSP00000513152.1:p.Ser371Tyr
ENST00000697164.1:c.1022C>A	ENSP00000513153.1:p.Ser341Tyr
ENST00000697165.1:c.809C>A	ENSP00000513154.1:p.Ser270Tyr
ENST00000697223.1:c.861C>A	ENSP00000513190.1:n.861C>A
ENST00000697224.1:c.884+3443C>A	ENSP00000513191.1:n.884+3443C>A
ENST00000697225.1:c.715C>A	ENSP00000513192.1:n.715C>A
ENST00000697226.1:c.738+3443C>A	ENSP00000513193.1:n.738+3443C>A
ENST00000697227.1:c.948C>A	ENSP00000513194.1:n.948C>A
ENST00000697228.1:c.804C>A	ENSP00000513195.1:n.804C>A
ENST00000697229.1:c.885-15592C>A	ENSP00000513196.1:n.885-15592C>A
ENST00000697230.1:c.1022C>A	ENSP00000513197.1:p.Ser341Tyr
ENST00000697231.1:c.1017C>A	ENSP00000513198.1:n.1017C>A
ENST00000697232.1:c.1041C>A	ENSP00000513199.1:n.1041C>A
ENST00000347310.10:c.1112C>A MANE Select	ENSP00000321345.5:p.Ser371Tyr
ENST00000637002.1:c.503C>A	ENSP00000490340.1:p.Ser168Tyr
ENST00000347310.9:c.1112C>A	ENSP00000321345.5:p.Ser371Tyr
ENST00000395227.2:c.-58-15592C>A	ENSP00000378652.2:n.-58-15592C>A
ENST00000425614.3:c.347C>A	ENSP00000387640.2:p.Ser116Tyr
ENST00000473881.2:c.191-15592C>A	ENSP00000486667.1:n.191-15592C>A
NM_144701.2:c.1112C>A	NP_653302.2:p.Ser371Tyr
XM_005270516.2:c.350C>A	XP_005270573.1:p.Ser117Tyr
XM_011540789.1:c.1202C>A	XP_011539091.1:p.Ser401Tyr
XM_011540790.1:c.1112C>A	XP_011539092.1:p.Ser371Tyr
XM_011540791.1:c.1112C>A	XP_011539093.1:p.Ser371Tyr
XM_011540790.3:c.1112C>A	XP_011539092.1:p.Ser371Tyr
XM_011540791.3:c.1112C>A	XP_011539093.1:p.Ser371Tyr
XR_001736993.1:n.1228+3443C>A
NM_144701.3:c.1112C>A MANE Select	NP_653302.2:p.Ser371Tyr