Canonical Allele Identifier: CA1173064261

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258777T= , CM000663.2:g.67258777T=	GRCh38
NC_000001.10:g.67724460T= , CM000663.1:g.67724460T=	GRCh37
NC_000001.9:g.67497048T=	NCBI36
NG_011498.1:g.97292T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1378T=	ENSP00000513138.1:n.1378T=
ENST00000697150.1:c.1436T=	ENSP00000513139.1:n.1436T=
ENST00000697151.1:c.1369T=	ENSP00000513140.1:n.1369T=
ENST00000697164.1:c.1449T=	ENSP00000513153.1:p.Val483=
ENST00000697165.1:c.1236T=	ENSP00000513154.1:p.Val412=
ENST00000347310.10:c.1539T= MANE Select	ENSP00000321345.5:p.Val513=
ENST00000637002.1:c.930T=	ENSP00000490340.1:p.Val310=
ENST00000347310.9:c.1539T=	ENSP00000321345.5:p.Val513=
ENST00000395227.2:c.333T=	ENSP00000378652.2:p.Val111=
ENST00000425614.3:c.774T=	ENSP00000387640.2:p.Val258=
ENST00000473881.2:c.*365T=	ENSP00000486667.1:n.*365T=
NM_144701.2:c.1539T=	NP_653302.2:p.Val513=
XM_005270516.2:c.777T=	XP_005270573.1:p.Val259=
XM_011540789.1:c.1629T=	XP_011539091.1:p.Val543=
XM_011540790.1:c.1539T=	XP_011539092.1:p.Val513=
XM_011540791.1:c.1539T=	XP_011539093.1:p.Val513=
XM_011540790.3:c.1539T=	XP_011539092.1:p.Val513=
XM_011540791.3:c.1539T=	XP_011539093.1:p.Val513=
XR_001736993.1:n.1619T=
NM_144701.3:c.1539T= MANE Select	NP_653302.2:p.Val513=