Canonical Allele Identifier: CA2516446405

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259088_67259089dup , CM000663.2:g.67259088_67259089dup	GRCh38
NC_000001.10:g.67724771_67724772dup , CM000663.1:g.67724771_67724772dup	GRCh37
NC_000001.9:g.67497359_67497360dup	NCBI36
NG_011498.1:g.97603_97604dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1689_1690dup	ENSP00000513138.1:n.1689_1690dup
ENST00000697150.1:c.1747_1748dup	ENSP00000513139.1:n.1747_1748dup
ENST00000697151.1:c.1680_1681dup	ENSP00000513140.1:n.1680_1681dup
ENST00000697164.1:c.1760_1761dup	ENSP00000513153.1:p.Glu588TrpfsTer?
ENST00000697165.1:c.1547_1548dup	ENSP00000513154.1:p.Glu517TrpfsTer?
ENST00000347310.10:c.1850_1851dup MANE Select	ENSP00000321345.5:p.Glu618TrpfsTer22
ENST00000637002.1:c.1241_1242dup	ENSP00000490340.1:p.Glu415TrpfsTer22
ENST00000347310.9:c.1850_1851dup	ENSP00000321345.5:p.Glu618TrpfsTer22
ENST00000395227.2:c.644_645dup	ENSP00000378652.2:p.Glu216TrpfsTer22
ENST00000425614.3:c.1085_1086dup	ENSP00000387640.2:p.Glu363TrpfsTer22
ENST00000473881.2:c.*676_*677dup	ENSP00000486667.1:n.*676_*677dup
NM_144701.2:c.1850_1851dup	NP_653302.2:p.Glu618TrpfsTer22
XM_005270516.2:c.1088_1089dup	XP_005270573.1:p.Glu364TrpfsTer22
XM_011540789.1:c.1940_1941dup	XP_011539091.1:p.Glu648TrpfsTer22
XM_011540790.1:c.1850_1851dup	XP_011539092.1:p.Glu618TrpfsTer22
XM_011540791.1:c.1850_1851dup	XP_011539093.1:p.Glu618TrpfsTer22
XM_011540790.3:c.1850_1851dup	XP_011539092.1:p.Glu618TrpfsTer22
XM_011540791.3:c.1850_1851dup	XP_011539093.1:p.Glu618TrpfsTer22
XR_001736993.1:n.1930_1931dup
NM_144701.3:c.1850_1851dup MANE Select	NP_653302.2:p.Glu618TrpfsTer22