Canonical Allele Identifier: CA1141248181

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258829G= , CM000663.2:g.67258829G=	GRCh38
NC_000001.10:g.67724512G= , CM000663.1:g.67724512G=	GRCh37
NC_000001.9:g.67497100G=	NCBI36
NG_011498.1:g.97344G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1430G=	ENSP00000513138.1:n.1430G=
ENST00000697150.1:c.1488G=	ENSP00000513139.1:n.1488G=
ENST00000697151.1:c.1421G=	ENSP00000513140.1:n.1421G=
ENST00000697164.1:c.1501G=	ENSP00000513153.1:p.Ala501=
ENST00000697165.1:c.1288G=	ENSP00000513154.1:p.Ala430=
ENST00000347310.10:c.1591G= MANE Select	ENSP00000321345.5:p.Ala531=
ENST00000637002.1:c.982G=	ENSP00000490340.1:p.Ala328=
ENST00000347310.9:c.1591G=	ENSP00000321345.5:p.Ala531=
ENST00000395227.2:c.385G=	ENSP00000378652.2:p.Ala129=
ENST00000425614.3:c.826G=	ENSP00000387640.2:p.Ala276=
ENST00000473881.2:c.*417G=	ENSP00000486667.1:n.*417G=
NM_144701.2:c.1591G=	NP_653302.2:p.Ala531=
XM_005270516.2:c.829G=	XP_005270573.1:p.Ala277=
XM_011540789.1:c.1681G=	XP_011539091.1:p.Ala561=
XM_011540790.1:c.1591G=	XP_011539092.1:p.Ala531=
XM_011540791.1:c.1591G=	XP_011539093.1:p.Ala531=
XM_011540790.3:c.1591G=	XP_011539092.1:p.Ala531=
XM_011540791.3:c.1591G=	XP_011539093.1:p.Ala531=
XR_001736993.1:n.1671G=
NM_144701.3:c.1591G= MANE Select	NP_653302.2:p.Ala531=