Canonical Allele Identifier: CA1173064300

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258929A= , CM000663.2:g.67258929A=	GRCh38
NC_000001.10:g.67724612A= , CM000663.1:g.67724612A=	GRCh37
NC_000001.9:g.67497200A=	NCBI36
NG_011498.1:g.97444A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1530A=	ENSP00000513138.1:n.1530A=
ENST00000697150.1:c.1588A=	ENSP00000513139.1:n.1588A=
ENST00000697151.1:c.1521A=	ENSP00000513140.1:n.1521A=
ENST00000697164.1:c.1601A=	ENSP00000513153.1:p.Gln534=
ENST00000697165.1:c.1388A=	ENSP00000513154.1:p.Gln463=
ENST00000347310.10:c.1691A= MANE Select	ENSP00000321345.5:p.Gln564=
ENST00000637002.1:c.1082A=	ENSP00000490340.1:p.Gln361=
ENST00000347310.9:c.1691A=	ENSP00000321345.5:p.Gln564=
ENST00000395227.2:c.485A=	ENSP00000378652.2:p.Gln162=
ENST00000425614.3:c.926A=	ENSP00000387640.2:p.Gln309=
ENST00000473881.2:c.*517A=	ENSP00000486667.1:n.*517A=
NM_144701.2:c.1691A=	NP_653302.2:p.Gln564=
XM_005270516.2:c.929A=	XP_005270573.1:p.Gln310=
XM_011540789.1:c.1781A=	XP_011539091.1:p.Gln594=
XM_011540790.1:c.1691A=	XP_011539092.1:p.Gln564=
XM_011540791.1:c.1691A=	XP_011539093.1:p.Gln564=
XM_011540790.3:c.1691A=	XP_011539092.1:p.Gln564=
XM_011540791.3:c.1691A=	XP_011539093.1:p.Gln564=
XR_001736993.1:n.1771A=
NM_144701.3:c.1691A= MANE Select	NP_653302.2:p.Gln564=