Canonical Allele Identifier: CA1173064270

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258823A= , CM000663.2:g.67258823A=	GRCh38
NC_000001.10:g.67724506A= , CM000663.1:g.67724506A=	GRCh37
NC_000001.9:g.67497094A=	NCBI36
NG_011498.1:g.97338A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1424A=	ENSP00000513138.1:n.1424A=
ENST00000697150.1:c.1482A=	ENSP00000513139.1:n.1482A=
ENST00000697151.1:c.1415A=	ENSP00000513140.1:n.1415A=
ENST00000697164.1:c.1495A=	ENSP00000513153.1:p.Asn499=
ENST00000697165.1:c.1282A=	ENSP00000513154.1:p.Asn428=
ENST00000347310.10:c.1585A= MANE Select	ENSP00000321345.5:p.Asn529=
ENST00000637002.1:c.976A=	ENSP00000490340.1:p.Asn326=
ENST00000347310.9:c.1585A=	ENSP00000321345.5:p.Asn529=
ENST00000395227.2:c.379A=	ENSP00000378652.2:p.Asn127=
ENST00000425614.3:c.820A=	ENSP00000387640.2:p.Asn274=
ENST00000473881.2:c.*411A=	ENSP00000486667.1:n.*411A=
NM_144701.2:c.1585A=	NP_653302.2:p.Asn529=
XM_005270516.2:c.823A=	XP_005270573.1:p.Asn275=
XM_011540789.1:c.1675A=	XP_011539091.1:p.Asn559=
XM_011540790.1:c.1585A=	XP_011539092.1:p.Asn529=
XM_011540791.1:c.1585A=	XP_011539093.1:p.Asn529=
XM_011540790.3:c.1585A=	XP_011539092.1:p.Asn529=
XM_011540791.3:c.1585A=	XP_011539093.1:p.Asn529=
XR_001736993.1:n.1665A=
NM_144701.3:c.1585A= MANE Select	NP_653302.2:p.Asn529=