Canonical Allele Identifier: CA1173064346

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259082A= , CM000663.2:g.67259082A=	GRCh38
NC_000001.10:g.67724765A= , CM000663.1:g.67724765A=	GRCh37
NC_000001.9:g.67497353A=	NCBI36
NG_011498.1:g.97597A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1683A=	ENSP00000513138.1:n.1683A=
ENST00000697150.1:c.1741A=	ENSP00000513139.1:n.1741A=
ENST00000697151.1:c.1674A=	ENSP00000513140.1:n.1674A=
ENST00000697164.1:c.1754A=	ENSP00000513153.1:p.Asn585=
ENST00000697165.1:c.1541A=	ENSP00000513154.1:p.Asn514=
ENST00000347310.10:c.1844A= MANE Select	ENSP00000321345.5:p.Asn615=
ENST00000637002.1:c.1235A=	ENSP00000490340.1:p.Asn412=
ENST00000347310.9:c.1844A=	ENSP00000321345.5:p.Asn615=
ENST00000395227.2:c.638A=	ENSP00000378652.2:p.Asn213=
ENST00000425614.3:c.1079A=	ENSP00000387640.2:p.Asn360=
ENST00000473881.2:c.*670A=	ENSP00000486667.1:n.*670A=
NM_144701.2:c.1844A=	NP_653302.2:p.Asn615=
XM_005270516.2:c.1082A=	XP_005270573.1:p.Asn361=
XM_011540789.1:c.1934A=	XP_011539091.1:p.Asn645=
XM_011540790.1:c.1844A=	XP_011539092.1:p.Asn615=
XM_011540791.1:c.1844A=	XP_011539093.1:p.Asn615=
XM_011540790.3:c.1844A=	XP_011539092.1:p.Asn615=
XM_011540791.3:c.1844A=	XP_011539093.1:p.Asn615=
XR_001736993.1:n.1924A=
NM_144701.3:c.1844A= MANE Select	NP_653302.2:p.Asn615=