Canonical Allele Identifier: CA1173064281

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258875T= , CM000663.2:g.67258875T=	GRCh38
NC_000001.10:g.67724558T= , CM000663.1:g.67724558T=	GRCh37
NC_000001.9:g.67497146T=	NCBI36
NG_011498.1:g.97390T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1476T=	ENSP00000513138.1:n.1476T=
ENST00000697150.1:c.1534T=	ENSP00000513139.1:n.1534T=
ENST00000697151.1:c.1467T=	ENSP00000513140.1:n.1467T=
ENST00000697164.1:c.1547T=	ENSP00000513153.1:p.Leu516=
ENST00000697165.1:c.1334T=	ENSP00000513154.1:p.Leu445=
ENST00000347310.10:c.1637T= MANE Select	ENSP00000321345.5:p.Leu546=
ENST00000637002.1:c.1028T=	ENSP00000490340.1:p.Leu343=
ENST00000347310.9:c.1637T=	ENSP00000321345.5:p.Leu546=
ENST00000395227.2:c.431T=	ENSP00000378652.2:p.Leu144=
ENST00000425614.3:c.872T=	ENSP00000387640.2:p.Leu291=
ENST00000473881.2:c.*463T=	ENSP00000486667.1:n.*463T=
NM_144701.2:c.1637T=	NP_653302.2:p.Leu546=
XM_005270516.2:c.875T=	XP_005270573.1:p.Leu292=
XM_011540789.1:c.1727T=	XP_011539091.1:p.Leu576=
XM_011540790.1:c.1637T=	XP_011539092.1:p.Leu546=
XM_011540791.1:c.1637T=	XP_011539093.1:p.Leu546=
XM_011540790.3:c.1637T=	XP_011539092.1:p.Leu546=
XM_011540791.3:c.1637T=	XP_011539093.1:p.Leu546=
XR_001736993.1:n.1717T=
NM_144701.3:c.1637T= MANE Select	NP_653302.2:p.Leu546=