Canonical Allele Identifier: CA1173064323

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259004T= , CM000663.2:g.67259004T=	GRCh38
NC_000001.10:g.67724687T= , CM000663.1:g.67724687T=	GRCh37
NC_000001.9:g.67497275T=	NCBI36
NG_011498.1:g.97519T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1605T=	ENSP00000513138.1:n.1605T=
ENST00000697150.1:c.1663T=	ENSP00000513139.1:n.1663T=
ENST00000697151.1:c.1596T=	ENSP00000513140.1:n.1596T=
ENST00000697164.1:c.1676T=	ENSP00000513153.1:p.Leu559=
ENST00000697165.1:c.1463T=	ENSP00000513154.1:p.Leu488=
ENST00000347310.10:c.1766T= MANE Select	ENSP00000321345.5:p.Leu589=
ENST00000637002.1:c.1157T=	ENSP00000490340.1:p.Leu386=
ENST00000347310.9:c.1766T=	ENSP00000321345.5:p.Leu589=
ENST00000395227.2:c.560T=	ENSP00000378652.2:p.Leu187=
ENST00000425614.3:c.1001T=	ENSP00000387640.2:p.Leu334=
ENST00000473881.2:c.*592T=	ENSP00000486667.1:n.*592T=
NM_144701.2:c.1766T=	NP_653302.2:p.Leu589=
XM_005270516.2:c.1004T=	XP_005270573.1:p.Leu335=
XM_011540789.1:c.1856T=	XP_011539091.1:p.Leu619=
XM_011540790.1:c.1766T=	XP_011539092.1:p.Leu589=
XM_011540791.1:c.1766T=	XP_011539093.1:p.Leu589=
XM_011540790.3:c.1766T=	XP_011539092.1:p.Leu589=
XM_011540791.3:c.1766T=	XP_011539093.1:p.Leu589=
XR_001736993.1:n.1846T=
NM_144701.3:c.1766T= MANE Select	NP_653302.2:p.Leu589=