Canonical Allele Identifier: CA1173064267

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258811C= , CM000663.2:g.67258811C=	GRCh38
NC_000001.10:g.67724494C= , CM000663.1:g.67724494C=	GRCh37
NC_000001.9:g.67497082C=	NCBI36
NG_011498.1:g.97326C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1412C=	ENSP00000513138.1:n.1412C=
ENST00000697150.1:c.1470C=	ENSP00000513139.1:n.1470C=
ENST00000697151.1:c.1403C=	ENSP00000513140.1:n.1403C=
ENST00000697164.1:c.1483C=	ENSP00000513153.1:p.Gln495=
ENST00000697165.1:c.1270C=	ENSP00000513154.1:p.Gln424=
ENST00000347310.10:c.1573C= MANE Select	ENSP00000321345.5:p.Gln525=
ENST00000637002.1:c.964C=	ENSP00000490340.1:p.Gln322=
ENST00000347310.9:c.1573C=	ENSP00000321345.5:p.Gln525=
ENST00000395227.2:c.367C=	ENSP00000378652.2:p.Gln123=
ENST00000425614.3:c.808C=	ENSP00000387640.2:p.Gln270=
ENST00000473881.2:c.*399C=	ENSP00000486667.1:n.*399C=
NM_144701.2:c.1573C=	NP_653302.2:p.Gln525=
XM_005270516.2:c.811C=	XP_005270573.1:p.Gln271=
XM_011540789.1:c.1663C=	XP_011539091.1:p.Gln555=
XM_011540790.1:c.1573C=	XP_011539092.1:p.Gln525=
XM_011540791.1:c.1573C=	XP_011539093.1:p.Gln525=
XM_011540790.3:c.1573C=	XP_011539092.1:p.Gln525=
XM_011540791.3:c.1573C=	XP_011539093.1:p.Gln525=
XR_001736993.1:n.1653C=
NM_144701.3:c.1573C= MANE Select	NP_653302.2:p.Gln525=