Canonical Allele Identifier: CA1173064246

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258732C= , CM000663.2:g.67258732C=	GRCh38
NC_000001.10:g.67724415C= , CM000663.1:g.67724415C=	GRCh37
NC_000001.9:g.67497003C=	NCBI36
NG_011498.1:g.97247C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1333C=	ENSP00000513138.1:n.1333C=
ENST00000697150.1:c.1391C=	ENSP00000513139.1:n.1391C=
ENST00000697151.1:c.1324C=	ENSP00000513140.1:n.1324C=
ENST00000697164.1:c.1404C=	ENSP00000513153.1:p.Leu468=
ENST00000697165.1:c.1191C=	ENSP00000513154.1:p.Leu397=
ENST00000347310.10:c.1494C= MANE Select	ENSP00000321345.5:p.Leu498=
ENST00000637002.1:c.885C=	ENSP00000490340.1:p.Leu295=
ENST00000347310.9:c.1494C=	ENSP00000321345.5:p.Leu498=
ENST00000395227.2:c.288C=	ENSP00000378652.2:p.Leu96=
ENST00000425614.3:c.729C=	ENSP00000387640.2:p.Leu243=
ENST00000473881.2:c.*320C=	ENSP00000486667.1:n.*320C=
NM_144701.2:c.1494C=	NP_653302.2:p.Leu498=
XM_005270516.2:c.732C=	XP_005270573.1:p.Leu244=
XM_011540789.1:c.1584C=	XP_011539091.1:p.Leu528=
XM_011540790.1:c.1494C=	XP_011539092.1:p.Leu498=
XM_011540791.1:c.1494C=	XP_011539093.1:p.Leu498=
XM_011540790.3:c.1494C=	XP_011539092.1:p.Leu498=
XM_011540791.3:c.1494C=	XP_011539093.1:p.Leu498=
XR_001736993.1:n.1574C=
NM_144701.3:c.1494C= MANE Select	NP_653302.2:p.Leu498=