Canonical Allele Identifier: CA1173064344

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259079A= , CM000663.2:g.67259079A=	GRCh38
NC_000001.10:g.67724762A= , CM000663.1:g.67724762A=	GRCh37
NC_000001.9:g.67497350A=	NCBI36
NG_011498.1:g.97594A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1680A=	ENSP00000513138.1:n.1680A=
ENST00000697150.1:c.1738A=	ENSP00000513139.1:n.1738A=
ENST00000697151.1:c.1671A=	ENSP00000513140.1:n.1671A=
ENST00000697164.1:c.1751A=	ENSP00000513153.1:p.Gln584=
ENST00000697165.1:c.1538A=	ENSP00000513154.1:p.Gln513=
ENST00000347310.10:c.1841A= MANE Select	ENSP00000321345.5:p.Gln614=
ENST00000637002.1:c.1232A=	ENSP00000490340.1:p.Gln411=
ENST00000347310.9:c.1841A=	ENSP00000321345.5:p.Gln614=
ENST00000395227.2:c.635A=	ENSP00000378652.2:p.Gln212=
ENST00000425614.3:c.1076A=	ENSP00000387640.2:p.Gln359=
ENST00000473881.2:c.*667A=	ENSP00000486667.1:n.*667A=
NM_144701.2:c.1841A=	NP_653302.2:p.Gln614=
XM_005270516.2:c.1079A=	XP_005270573.1:p.Gln360=
XM_011540789.1:c.1931A=	XP_011539091.1:p.Gln644=
XM_011540790.1:c.1841A=	XP_011539092.1:p.Gln614=
XM_011540791.1:c.1841A=	XP_011539093.1:p.Gln614=
XM_011540790.3:c.1841A=	XP_011539092.1:p.Gln614=
XM_011540791.3:c.1841A=	XP_011539093.1:p.Gln614=
XR_001736993.1:n.1921A=
NM_144701.3:c.1841A= MANE Select	NP_653302.2:p.Gln614=