Canonical Allele Identifier: CA1173064262

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258779A= , CM000663.2:g.67258779A=	GRCh38
NC_000001.10:g.67724462A= , CM000663.1:g.67724462A=	GRCh37
NC_000001.9:g.67497050A=	NCBI36
NG_011498.1:g.97294A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1380A=	ENSP00000513138.1:n.1380A=
ENST00000697150.1:c.1438A=	ENSP00000513139.1:n.1438A=
ENST00000697151.1:c.1371A=	ENSP00000513140.1:n.1371A=
ENST00000697164.1:c.1451A=	ENSP00000513153.1:p.Asp484=
ENST00000697165.1:c.1238A=	ENSP00000513154.1:p.Asp413=
ENST00000347310.10:c.1541A= MANE Select	ENSP00000321345.5:p.Asp514=
ENST00000637002.1:c.932A=	ENSP00000490340.1:p.Asp311=
ENST00000347310.9:c.1541A=	ENSP00000321345.5:p.Asp514=
ENST00000395227.2:c.335A=	ENSP00000378652.2:p.Asp112=
ENST00000425614.3:c.776A=	ENSP00000387640.2:p.Asp259=
ENST00000473881.2:c.*367A=	ENSP00000486667.1:n.*367A=
NM_144701.2:c.1541A=	NP_653302.2:p.Asp514=
XM_005270516.2:c.779A=	XP_005270573.1:p.Asp260=
XM_011540789.1:c.1631A=	XP_011539091.1:p.Asp544=
XM_011540790.1:c.1541A=	XP_011539092.1:p.Asp514=
XM_011540791.1:c.1541A=	XP_011539093.1:p.Asp514=
XM_011540790.3:c.1541A=	XP_011539092.1:p.Asp514=
XM_011540791.3:c.1541A=	XP_011539093.1:p.Asp514=
XR_001736993.1:n.1621A=
NM_144701.3:c.1541A= MANE Select	NP_653302.2:p.Asp514=