Canonical Allele Identifier: CA1143915460

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258790T= , CM000663.2:g.67258790T=	GRCh38
NC_000001.10:g.67724473T= , CM000663.1:g.67724473T=	GRCh37
NC_000001.9:g.67497061T=	NCBI36
NG_011498.1:g.97305T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1391T=	ENSP00000513138.1:n.1391T=
ENST00000697150.1:c.1449T=	ENSP00000513139.1:n.1449T=
ENST00000697151.1:c.1382T=	ENSP00000513140.1:n.1382T=
ENST00000697164.1:c.1462T=	ENSP00000513153.1:p.Ser488=
ENST00000697165.1:c.1249T=	ENSP00000513154.1:p.Ser417=
ENST00000347310.10:c.1552T= MANE Select	ENSP00000321345.5:p.Ser518=
ENST00000637002.1:c.943T=	ENSP00000490340.1:p.Ser315=
ENST00000347310.9:c.1552T=	ENSP00000321345.5:p.Ser518=
ENST00000395227.2:c.346T=	ENSP00000378652.2:p.Ser116=
ENST00000425614.3:c.787T=	ENSP00000387640.2:p.Ser263=
ENST00000473881.2:c.*378T=	ENSP00000486667.1:n.*378T=
NM_144701.2:c.1552T=	NP_653302.2:p.Ser518=
XM_005270516.2:c.790T=	XP_005270573.1:p.Ser264=
XM_011540789.1:c.1642T=	XP_011539091.1:p.Ser548=
XM_011540790.1:c.1552T=	XP_011539092.1:p.Ser518=
XM_011540791.1:c.1552T=	XP_011539093.1:p.Ser518=
XM_011540790.3:c.1552T=	XP_011539092.1:p.Ser518=
XM_011540791.3:c.1552T=	XP_011539093.1:p.Ser518=
XR_001736993.1:n.1632T=
NM_144701.3:c.1552T= MANE Select	NP_653302.2:p.Ser518=