Canonical Allele Identifier: CA1173064279

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258868A= , CM000663.2:g.67258868A=	GRCh38
NC_000001.10:g.67724551A= , CM000663.1:g.67724551A=	GRCh37
NC_000001.9:g.67497139A=	NCBI36
NG_011498.1:g.97383A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1469A=	ENSP00000513138.1:n.1469A=
ENST00000697150.1:c.1527A=	ENSP00000513139.1:n.1527A=
ENST00000697151.1:c.1460A=	ENSP00000513140.1:n.1460A=
ENST00000697164.1:c.1540A=	ENSP00000513153.1:p.Ile514=
ENST00000697165.1:c.1327A=	ENSP00000513154.1:p.Ile443=
ENST00000347310.10:c.1630A= MANE Select	ENSP00000321345.5:p.Ile544=
ENST00000637002.1:c.1021A=	ENSP00000490340.1:p.Ile341=
ENST00000347310.9:c.1630A=	ENSP00000321345.5:p.Ile544=
ENST00000395227.2:c.424A=	ENSP00000378652.2:p.Ile142=
ENST00000425614.3:c.865A=	ENSP00000387640.2:p.Ile289=
ENST00000473881.2:c.*456A=	ENSP00000486667.1:n.*456A=
NM_144701.2:c.1630A=	NP_653302.2:p.Ile544=
XM_005270516.2:c.868A=	XP_005270573.1:p.Ile290=
XM_011540789.1:c.1720A=	XP_011539091.1:p.Ile574=
XM_011540790.1:c.1630A=	XP_011539092.1:p.Ile544=
XM_011540791.1:c.1630A=	XP_011539093.1:p.Ile544=
XM_011540790.3:c.1630A=	XP_011539092.1:p.Ile544=
XM_011540791.3:c.1630A=	XP_011539093.1:p.Ile544=
XR_001736993.1:n.1710A=
NM_144701.3:c.1630A= MANE Select	NP_653302.2:p.Ile544=