Canonical Allele Identifier: CA1173064348

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259087T= , CM000663.2:g.67259087T=	GRCh38
NC_000001.10:g.67724770T= , CM000663.1:g.67724770T=	GRCh37
NC_000001.9:g.67497358T=	NCBI36
NG_011498.1:g.97602T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1688T=	ENSP00000513138.1:n.1688T=
ENST00000697150.1:c.1746T=	ENSP00000513139.1:n.1746T=
ENST00000697151.1:c.1679T=	ENSP00000513140.1:n.1679T=
ENST00000697164.1:c.1759T=	ENSP00000513153.1:p.Leu587=
ENST00000697165.1:c.1546T=	ENSP00000513154.1:p.Leu516=
ENST00000347310.10:c.1849T= MANE Select	ENSP00000321345.5:p.Leu617=
ENST00000637002.1:c.1240T=	ENSP00000490340.1:p.Leu414=
ENST00000347310.9:c.1849T=	ENSP00000321345.5:p.Leu617=
ENST00000395227.2:c.643T=	ENSP00000378652.2:p.Leu215=
ENST00000425614.3:c.1084T=	ENSP00000387640.2:p.Leu362=
ENST00000473881.2:c.*675T=	ENSP00000486667.1:n.*675T=
NM_144701.2:c.1849T=	NP_653302.2:p.Leu617=
XM_005270516.2:c.1087T=	XP_005270573.1:p.Leu363=
XM_011540789.1:c.1939T=	XP_011539091.1:p.Leu647=
XM_011540790.1:c.1849T=	XP_011539092.1:p.Leu617=
XM_011540791.1:c.1849T=	XP_011539093.1:p.Leu617=
XM_011540790.3:c.1849T=	XP_011539092.1:p.Leu617=
XM_011540791.3:c.1849T=	XP_011539093.1:p.Leu617=
XR_001736993.1:n.1929T=
NM_144701.3:c.1849T= MANE Select	NP_653302.2:p.Leu617=