Canonical Allele Identifier: CA2646125923

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259036-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259037del , CM000663.2:g.67259037del	GRCh38
NC_000001.10:g.67724720del , CM000663.1:g.67724720del	GRCh37
NC_000001.9:g.67497308del	NCBI36
NG_011498.1:g.97552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1638del	ENSP00000513138.1:n.1638del
ENST00000697150.1:c.1696del	ENSP00000513139.1:n.1696del
ENST00000697151.1:c.1629del	ENSP00000513140.1:n.1629del
ENST00000697164.1:c.1709del	ENSP00000513153.1:p.Ile570ThrfsTer2
ENST00000697165.1:c.1496del	ENSP00000513154.1:p.Ile499ThrfsTer2
ENST00000347310.10:c.1799del MANE Select	ENSP00000321345.5:p.Ile600ThrfsTer2
ENST00000637002.1:c.1190del	ENSP00000490340.1:p.Ile397ThrfsTer2
ENST00000347310.9:c.1799del	ENSP00000321345.5:p.Ile600ThrfsTer2
ENST00000395227.2:c.593del	ENSP00000378652.2:p.Ile198ThrfsTer2
ENST00000425614.3:c.1034del	ENSP00000387640.2:p.Ile345ThrfsTer2
ENST00000473881.2:c.*625del	ENSP00000486667.1:n.*625del
NM_144701.2:c.1799del	NP_653302.2:p.Ile600ThrfsTer2
XM_005270516.2:c.1037del	XP_005270573.1:p.Ile346ThrfsTer2
XM_011540789.1:c.1889del	XP_011539091.1:p.Ile630ThrfsTer2
XM_011540790.1:c.1799del	XP_011539092.1:p.Ile600ThrfsTer2
XM_011540791.1:c.1799del	XP_011539093.1:p.Ile600ThrfsTer2
XM_011540790.3:c.1799del	XP_011539092.1:p.Ile600ThrfsTer2
XM_011540791.3:c.1799del	XP_011539093.1:p.Ile600ThrfsTer2
XR_001736993.1:n.1879del
NM_144701.3:c.1799del MANE Select	NP_653302.2:p.Ile600ThrfsTer2