Canonical Allele Identifier: CA340729631
Community Standard Title: NM_144701.3(IL23R):c.1789T>A (p.Cys597Ser)
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259027T>A , CM000663.2:g.67259027T>A GRCh38
NC_000001.10:g.67724710T>A , CM000663.1:g.67724710T>A GRCh37
NC_000001.9:g.67497298T>A NCBI36
NG_011498.1:g.97542T>A

Transcript Alleles

HGVS Amino-acid Change
NM_144701.3:c.1789T>A MANE Select NP_653302.2:p.Cys597Ser
ENST00000347310.10:c.1789T>A MANE Select ENSP00000321345.5:p.Cys597Ser
NM_144701.2:c.1789T>A NP_653302.2:p.Cys597Ser
ENST00000347310.9:c.1789T>A ENSP00000321345.5:p.Cys597Ser
ENST00000395227.2:c.583T>A ENSP00000378652.2:p.Cys195Ser
ENST00000425614.3:c.1024T>A ENSP00000387640.2:p.Cys342Ser
ENST00000473881.2:c.*615T>A ENSP00000486667.1:n.*615T>A
ENST00000637002.1:c.1180T>A ENSP00000490340.1:p.Cys394Ser
ENST00000697149.1:c.1628T>A ENSP00000513138.1:n.1628T>A
ENST00000697150.1:c.1686T>A ENSP00000513139.1:n.1686T>A
ENST00000697151.1:c.1619T>A ENSP00000513140.1:n.1619T>A
ENST00000697164.1:c.1699T>A ENSP00000513153.1:p.Cys567Ser
ENST00000697165.1:c.1486T>A ENSP00000513154.1:p.Cys496Ser
XM_005270516.2:c.1027T>A XP_005270573.1:p.Cys343Ser
XM_011540789.1:c.1879T>A XP_011539091.1:p.Cys627Ser
XM_011540790.1:c.1789T>A XP_011539092.1:p.Cys597Ser
XM_011540790.3:c.1789T>A XP_011539092.1:p.Cys597Ser
XM_011540791.1:c.1789T>A XP_011539093.1:p.Cys597Ser
XM_011540791.3:c.1789T>A XP_011539093.1:p.Cys597Ser
XR_001736993.1:n.1869T>A