Canonical Allele Identifier: CA2574401292

Gene: IL23R C1orf141

Linked Data

• ClinVar Variation Id: 1956091
• ClinVar RCV Id: RCV002700580
• gnomAD v4: 1-67200718-CTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67200726_67200728del , CM000663.2:g.67200726_67200728del	GRCh38
NC_000001.10:g.67666409_67666411del , CM000663.1:g.67666409_67666411del	GRCh37
NC_000001.9:g.67438997_67438999del	NCBI36
NG_011498.1:g.39241_39243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697148.1:c.368-11_368-9del (IL23R)	ENSP00000513137.1:n.368-11_368-9del
ENST00000697149.1:c.492-6184_492-6182del (IL23R)	ENSP00000513138.1:n.492-6184_492-6182del
ENST00000697150.1:c.492-11_492-9del (IL23R)	ENSP00000513139.1:n.492-11_492-9del
ENST00000697151.1:c.492-11_492-9del (IL23R)	ENSP00000513140.1:n.492-11_492-9del
ENST00000697152.1:c.492-11_492-9del (IL23R)	ENSP00000513141.1:n.492-11_492-9del
ENST00000697153.1:c.492-6184_492-6182del (IL23R)	ENSP00000513142.1:n.492-6184_492-6182del
ENST00000697154.1:c.492-11_492-9del (IL23R)	ENSP00000513143.1:n.492-11_492-9del
ENST00000697155.1:c.491+17767_491+17769del (IL23R)	ENSP00000513144.1:n.491+17767_491+17769del
ENST00000697156.1:c.492-11_492-9del (IL23R)	ENSP00000513145.1:n.492-11_492-9del
ENST00000697157.1:c.492-11_492-9del (IL23R)	ENSP00000513146.1:n.492-11_492-9del
ENST00000697158.1:c.492-11_492-9del (IL23R)	ENSP00000513147.1:n.492-11_492-9del
ENST00000697159.1:c.491+17767_491+17769del (IL23R)	ENSP00000513148.1:n.491+17767_491+17769del
ENST00000697160.1:c.492-11_492-9del (IL23R)	ENSP00000513149.1:n.492-11_492-9del
ENST00000697161.1:c.491+17767_491+17769del (IL23R)	ENSP00000513150.1:n.491+17767_491+17769del
ENST00000697162.1:c.492-82_492-80del (IL23R)	ENSP00000513151.1:n.492-82_492-80del
ENST00000697163.1:c.492-11_492-9del (IL23R)	ENSP00000513152.1:n.492-11_492-9del
ENST00000697164.1:c.492-11_492-9del (IL23R)	ENSP00000513153.1:n.492-11_492-9del
ENST00000697165.1:c.492-11_492-9del (IL23R)	ENSP00000513154.1:n.492-11_492-9del
ENST00000697223.1:c.492-6184_492-6182del (IL23R)	ENSP00000513190.1:n.492-6184_492-6182del
ENST00000697224.1:c.492-6184_492-6182del (IL23R)	ENSP00000513191.1:n.492-6184_492-6182del
ENST00000697225.1:c.491+17767_491+17769del (IL23R)	ENSP00000513192.1:n.491+17767_491+17769del
ENST00000697226.1:c.491+17767_491+17769del (IL23R)	ENSP00000513193.1:n.491+17767_491+17769del
ENST00000697227.1:c.492-11_492-9del (IL23R)	ENSP00000513194.1:n.492-11_492-9del
ENST00000697228.1:c.492-16_492-14del (IL23R)	ENSP00000513195.1:n.492-16_492-14del
ENST00000697229.1:c.492-82_492-80del (IL23R)	ENSP00000513196.1:n.492-82_492-80del
ENST00000697230.1:c.492-11_492-9del (IL23R)	ENSP00000513197.1:n.492-11_492-9del
ENST00000697231.1:c.492-16_492-14del (IL23R)	ENSP00000513198.1:n.492-16_492-14del
ENST00000697232.1:c.492-82_492-80del (IL23R)	ENSP00000513199.1:n.492-82_492-80del
ENST00000347310.10:c.492-11_492-9del (IL23R) MANE Select	ENSP00000321345.5:n.492-11_492-9del
ENST00000637002.1:c.-113-16_-113-14del (IL23R)	ENSP00000490340.1:n.-113-16_-113-14del
ENST00000347310.9:c.492-11_492-9del (IL23R)	ENSP00000321345.5:n.492-11_492-9del
ENST00000371007.6:c.-104+31125_-104+31127del (C1orf141)	ENSP00000360046.1:n.-104+31125_-104+31127del
ENST00000448166.6:c.-104+31125_-104+31127del (C1orf141)	ENSP00000415519.2:n.-104+31125_-104+31127del
NM_144701.2:c.492-11_492-9del (IL23R)	NP_653302.2:n.492-11_492-9del
XM_005270516.2:c.-110-6184_-110-6182del (IL23R)	XP_005270573.1:n.-110-6184_-110-6182del
XM_011540789.1:c.582-11_582-9del (IL23R)	XP_011539091.1:n.582-11_582-9del
XM_011540790.1:c.492-11_492-9del (IL23R)	XP_011539092.1:n.492-11_492-9del
XM_011540791.1:c.492-11_492-9del (IL23R)	XP_011539093.1:n.492-11_492-9del
XM_011540790.3:c.492-11_492-9del (IL23R)	XP_011539092.1:n.492-11_492-9del
XM_011540791.3:c.492-11_492-9del (IL23R)	XP_011539093.1:n.492-11_492-9del
XR_001736993.1:n.675-11_675-9del (IL23R)
NM_144701.3:c.492-11_492-9del (IL23R) MANE Select	NP_653302.2:n.492-11_492-9del