Canonical Allele Identifier: CA1173064307

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258955A= , CM000663.2:g.67258955A=	GRCh38
NC_000001.10:g.67724638A= , CM000663.1:g.67724638A=	GRCh37
NC_000001.9:g.67497226A=	NCBI36
NG_011498.1:g.97470A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1556A=	ENSP00000513138.1:n.1556A=
ENST00000697150.1:c.1614A=	ENSP00000513139.1:n.1614A=
ENST00000697151.1:c.1547A=	ENSP00000513140.1:n.1547A=
ENST00000697164.1:c.1627A=	ENSP00000513153.1:p.Met543=
ENST00000697165.1:c.1414A=	ENSP00000513154.1:p.Met472=
ENST00000347310.10:c.1717A= MANE Select	ENSP00000321345.5:p.Met573=
ENST00000637002.1:c.1108A=	ENSP00000490340.1:p.Met370=
ENST00000347310.9:c.1717A=	ENSP00000321345.5:p.Met573=
ENST00000395227.2:c.511A=	ENSP00000378652.2:p.Met171=
ENST00000425614.3:c.952A=	ENSP00000387640.2:p.Met318=
ENST00000473881.2:c.*543A=	ENSP00000486667.1:n.*543A=
NM_144701.2:c.1717A=	NP_653302.2:p.Met573=
XM_005270516.2:c.955A=	XP_005270573.1:p.Met319=
XM_011540789.1:c.1807A=	XP_011539091.1:p.Met603=
XM_011540790.1:c.1717A=	XP_011539092.1:p.Met573=
XM_011540791.1:c.1717A=	XP_011539093.1:p.Met573=
XM_011540790.3:c.1717A=	XP_011539092.1:p.Met573=
XM_011540791.3:c.1717A=	XP_011539093.1:p.Met573=
XR_001736993.1:n.1797A=
NM_144701.3:c.1717A= MANE Select	NP_653302.2:p.Met573=