Canonical Allele Identifier: CA418438691

Gene: IL23R

Linked Data

• COSMIC: COSM911827
• MyVariant Identifiers: chr1:g.67724466C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258783C>A , CM000663.2:g.67258783C>A	GRCh38
NC_000001.10:g.67724466C>A , CM000663.1:g.67724466C>A	GRCh37
NC_000001.9:g.67497054C>A	NCBI36
NG_011498.1:g.97298C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1384C>A	ENSP00000513138.1:n.1384C>A
ENST00000697150.1:c.1442C>A	ENSP00000513139.1:n.1442C>A
ENST00000697151.1:c.1375C>A	ENSP00000513140.1:n.1375C>A
ENST00000697164.1:c.1455C>A	ENSP00000513153.1:p.Ser485=
ENST00000697165.1:c.1242C>A	ENSP00000513154.1:p.Ser414=
ENST00000347310.10:c.1545C>A MANE Select	ENSP00000321345.5:p.Ser515=
ENST00000637002.1:c.936C>A	ENSP00000490340.1:p.Ser312=
ENST00000347310.9:c.1545C>A	ENSP00000321345.5:p.Ser515=
ENST00000395227.2:c.339C>A	ENSP00000378652.2:p.Ser113=
ENST00000425614.3:c.780C>A	ENSP00000387640.2:p.Ser260=
ENST00000473881.2:c.*371C>A	ENSP00000486667.1:n.*371C>A
NM_144701.2:c.1545C>A	NP_653302.2:p.Ser515=
XM_005270516.2:c.783C>A	XP_005270573.1:p.Ser261=
XM_011540789.1:c.1635C>A	XP_011539091.1:p.Ser545=
XM_011540790.1:c.1545C>A	XP_011539092.1:p.Ser515=
XM_011540791.1:c.1545C>A	XP_011539093.1:p.Ser515=
XM_011540790.3:c.1545C>A	XP_011539092.1:p.Ser515=
XM_011540791.3:c.1545C>A	XP_011539093.1:p.Ser515=
XR_001736993.1:n.1625C>A
NM_144701.3:c.1545C>A MANE Select	NP_653302.2:p.Ser515=