Canonical Allele Identifier: CA1173064257

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258766A= , CM000663.2:g.67258766A=	GRCh38
NC_000001.10:g.67724449A= , CM000663.1:g.67724449A=	GRCh37
NC_000001.9:g.67497037A=	NCBI36
NG_011498.1:g.97281A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1367A=	ENSP00000513138.1:n.1367A=
ENST00000697150.1:c.1425A=	ENSP00000513139.1:n.1425A=
ENST00000697151.1:c.1358A=	ENSP00000513140.1:n.1358A=
ENST00000697164.1:c.1438A=	ENSP00000513153.1:p.Lys480=
ENST00000697165.1:c.1225A=	ENSP00000513154.1:p.Lys409=
ENST00000347310.10:c.1528A= MANE Select	ENSP00000321345.5:p.Lys510=
ENST00000637002.1:c.919A=	ENSP00000490340.1:p.Lys307=
ENST00000347310.9:c.1528A=	ENSP00000321345.5:p.Lys510=
ENST00000395227.2:c.322A=	ENSP00000378652.2:p.Lys108=
ENST00000425614.3:c.763A=	ENSP00000387640.2:p.Lys255=
ENST00000473881.2:c.*354A=	ENSP00000486667.1:n.*354A=
NM_144701.2:c.1528A=	NP_653302.2:p.Lys510=
XM_005270516.2:c.766A=	XP_005270573.1:p.Lys256=
XM_011540789.1:c.1618A=	XP_011539091.1:p.Lys540=
XM_011540790.1:c.1528A=	XP_011539092.1:p.Lys510=
XM_011540791.1:c.1528A=	XP_011539093.1:p.Lys510=
XM_011540790.3:c.1528A=	XP_011539092.1:p.Lys510=
XM_011540791.3:c.1528A=	XP_011539093.1:p.Lys510=
XR_001736993.1:n.1608A=
NM_144701.3:c.1528A= MANE Select	NP_653302.2:p.Lys510=