Canonical Allele Identifier: CA1173064260

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258771A= , CM000663.2:g.67258771A=	GRCh38
NC_000001.10:g.67724454A= , CM000663.1:g.67724454A=	GRCh37
NC_000001.9:g.67497042A=	NCBI36
NG_011498.1:g.97286A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1372A=	ENSP00000513138.1:n.1372A=
ENST00000697150.1:c.1430A=	ENSP00000513139.1:n.1430A=
ENST00000697151.1:c.1363A=	ENSP00000513140.1:n.1363A=
ENST00000697164.1:c.1443A=	ENSP00000513153.1:p.Pro481=
ENST00000697165.1:c.1230A=	ENSP00000513154.1:p.Pro410=
ENST00000347310.10:c.1533A= MANE Select	ENSP00000321345.5:p.Pro511=
ENST00000637002.1:c.924A=	ENSP00000490340.1:p.Pro308=
ENST00000347310.9:c.1533A=	ENSP00000321345.5:p.Pro511=
ENST00000395227.2:c.327A=	ENSP00000378652.2:p.Pro109=
ENST00000425614.3:c.768A=	ENSP00000387640.2:p.Pro256=
ENST00000473881.2:c.*359A=	ENSP00000486667.1:n.*359A=
NM_144701.2:c.1533A=	NP_653302.2:p.Pro511=
XM_005270516.2:c.771A=	XP_005270573.1:p.Pro257=
XM_011540789.1:c.1623A=	XP_011539091.1:p.Pro541=
XM_011540790.1:c.1533A=	XP_011539092.1:p.Pro511=
XM_011540791.1:c.1533A=	XP_011539093.1:p.Pro511=
XM_011540790.3:c.1533A=	XP_011539092.1:p.Pro511=
XM_011540791.3:c.1533A=	XP_011539093.1:p.Pro511=
XR_001736993.1:n.1613A=
NM_144701.3:c.1533A= MANE Select	NP_653302.2:p.Pro511=