Canonical Allele Identifier: CA3081745143

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259123A= , CM000663.2:g.67259123A=	GRCh38
NC_000001.10:g.67724806A= , CM000663.1:g.67724806A=	GRCh37
NC_000001.9:g.67497394A=	NCBI36
NG_011498.1:g.97638A=

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1885A= MANE Select	NP_653302.2:p.Lys629=
ENST00000347310.10:c.1885A= MANE Select	ENSP00000321345.5:p.Lys629=
NM_144701.2:c.1885A=	NP_653302.2:p.Lys629=
ENST00000347310.9:c.1885A=	ENSP00000321345.5:p.Lys629=
ENST00000395227.2:c.679A=	ENSP00000378652.2:p.Lys227=
ENST00000425614.3:c.1120A=	ENSP00000387640.2:p.Lys374=
ENST00000473881.2:c.*711A=	ENSP00000486667.1:n.*711A=
ENST00000637002.1:c.1276A=	ENSP00000490340.1:p.Lys426=
ENST00000697149.1:c.1724A=	ENSP00000513138.1:n.1724A=
ENST00000697150.1:c.1782A=	ENSP00000513139.1:n.1782A=
ENST00000697151.1:c.1715A=	ENSP00000513140.1:n.1715A=
ENST00000697164.1:c.1795A=	ENSP00000513153.1:p.Lys599=
ENST00000697165.1:c.1582A=	ENSP00000513154.1:p.Lys528=
XM_005270516.2:c.1123A=	XP_005270573.1:p.Lys375=
XM_011540789.1:c.1975A=	XP_011539091.1:p.Lys659=
XM_011540790.1:c.1885A=	XP_011539092.1:p.Lys629=
XM_011540790.3:c.1885A=	XP_011539092.1:p.Lys629=
XM_011540791.1:c.1885A=	XP_011539093.1:p.Lys629=
XM_011540791.3:c.1885A=	XP_011539093.1:p.Lys629=
XR_001736993.1:n.1965A=