Canonical Allele Identifier: CA1173064268

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258816G= , CM000663.2:g.67258816G=	GRCh38
NC_000001.10:g.67724499G= , CM000663.1:g.67724499G=	GRCh37
NC_000001.9:g.67497087G=	NCBI36
NG_011498.1:g.97331G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1417G=	ENSP00000513138.1:n.1417G=
ENST00000697150.1:c.1475G=	ENSP00000513139.1:n.1475G=
ENST00000697151.1:c.1408G=	ENSP00000513140.1:n.1408G=
ENST00000697164.1:c.1488G=	ENSP00000513153.1:p.Lys496=
ENST00000697165.1:c.1275G=	ENSP00000513154.1:p.Lys425=
ENST00000347310.10:c.1578G= MANE Select	ENSP00000321345.5:p.Lys526=
ENST00000637002.1:c.969G=	ENSP00000490340.1:p.Lys323=
ENST00000347310.9:c.1578G=	ENSP00000321345.5:p.Lys526=
ENST00000395227.2:c.372G=	ENSP00000378652.2:p.Lys124=
ENST00000425614.3:c.813G=	ENSP00000387640.2:p.Lys271=
ENST00000473881.2:c.*404G=	ENSP00000486667.1:n.*404G=
NM_144701.2:c.1578G=	NP_653302.2:p.Lys526=
XM_005270516.2:c.816G=	XP_005270573.1:p.Lys272=
XM_011540789.1:c.1668G=	XP_011539091.1:p.Lys556=
XM_011540790.1:c.1578G=	XP_011539092.1:p.Lys526=
XM_011540791.1:c.1578G=	XP_011539093.1:p.Lys526=
XM_011540790.3:c.1578G=	XP_011539092.1:p.Lys526=
XM_011540791.3:c.1578G=	XP_011539093.1:p.Lys526=
XR_001736993.1:n.1658G=
NM_144701.3:c.1578G= MANE Select	NP_653302.2:p.Lys526=