Canonical Allele Identifier: CA340730121

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259114C>A , CM000663.2:g.67259114C>A	GRCh38
NC_000001.10:g.67724797C>A , CM000663.1:g.67724797C>A	GRCh37
NC_000001.9:g.67497385C>A	NCBI36
NG_011498.1:g.97629C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1876C>A MANE Select	NP_653302.2:p.Leu626Ile
ENST00000347310.10:c.1876C>A MANE Select	ENSP00000321345.5:p.Leu626Ile
NM_144701.2:c.1876C>A	NP_653302.2:p.Leu626Ile
ENST00000347310.9:c.1876C>A	ENSP00000321345.5:p.Leu626Ile
ENST00000395227.2:c.670C>A	ENSP00000378652.2:p.Leu224Ile
ENST00000425614.3:c.1111C>A	ENSP00000387640.2:p.Leu371Ile
ENST00000473881.2:c.*702C>A	ENSP00000486667.1:n.*702C>A
ENST00000637002.1:c.1267C>A	ENSP00000490340.1:p.Leu423Ile
ENST00000697149.1:c.1715C>A	ENSP00000513138.1:n.1715C>A
ENST00000697150.1:c.1773C>A	ENSP00000513139.1:n.1773C>A
ENST00000697151.1:c.1706C>A	ENSP00000513140.1:n.1706C>A
ENST00000697164.1:c.1786C>A	ENSP00000513153.1:p.Leu596Ile
ENST00000697165.1:c.1573C>A	ENSP00000513154.1:p.Leu525Ile
XM_005270516.2:c.1114C>A	XP_005270573.1:p.Leu372Ile
XM_011540789.1:c.1966C>A	XP_011539091.1:p.Leu656Ile
XM_011540790.1:c.1876C>A	XP_011539092.1:p.Leu626Ile
XM_011540790.3:c.1876C>A	XP_011539092.1:p.Leu626Ile
XM_011540791.1:c.1876C>A	XP_011539093.1:p.Leu626Ile
XM_011540791.3:c.1876C>A	XP_011539093.1:p.Leu626Ile
XR_001736993.1:n.1956C>A