Canonical Allele Identifier: CA340729650
Community Standard Title: NM_144701.3(IL23R):c.1793T>A (p.Leu598Ter)
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259031T>A , CM000663.2:g.67259031T>A GRCh38
NC_000001.10:g.67724714T>A , CM000663.1:g.67724714T>A GRCh37
NC_000001.9:g.67497302T>A NCBI36
NG_011498.1:g.97546T>A

Transcript Alleles

HGVS Amino-acid Change
NM_144701.3:c.1793T>A MANE Select NP_653302.2:p.Leu598Ter
ENST00000347310.10:c.1793T>A MANE Select ENSP00000321345.5:p.Leu598Ter
NM_144701.2:c.1793T>A NP_653302.2:p.Leu598Ter
ENST00000347310.9:c.1793T>A ENSP00000321345.5:p.Leu598Ter
ENST00000395227.2:c.587T>A ENSP00000378652.2:p.Leu196Ter
ENST00000425614.3:c.1028T>A ENSP00000387640.2:p.Leu343Ter
ENST00000473881.2:c.*619T>A ENSP00000486667.1:n.*619T>A
ENST00000637002.1:c.1184T>A ENSP00000490340.1:p.Leu395Ter
ENST00000697149.1:c.1632T>A ENSP00000513138.1:n.1632T>A
ENST00000697150.1:c.1690T>A ENSP00000513139.1:n.1690T>A
ENST00000697151.1:c.1623T>A ENSP00000513140.1:n.1623T>A
ENST00000697164.1:c.1703T>A ENSP00000513153.1:p.Leu568Ter
ENST00000697165.1:c.1490T>A ENSP00000513154.1:p.Leu497Ter
XM_005270516.2:c.1031T>A XP_005270573.1:p.Leu344Ter
XM_011540789.1:c.1883T>A XP_011539091.1:p.Leu628Ter
XM_011540790.1:c.1793T>A XP_011539092.1:p.Leu598Ter
XM_011540790.3:c.1793T>A XP_011539092.1:p.Leu598Ter
XM_011540791.1:c.1793T>A XP_011539093.1:p.Leu598Ter
XM_011540791.3:c.1793T>A XP_011539093.1:p.Leu598Ter
XR_001736993.1:n.1873T>A