Canonical Allele Identifier: CA738095244

Gene: IL23R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259178_67259189del , CM000663.2:g.67259178_67259189del	GRCh38
NC_000001.10:g.67724861_67724872del , CM000663.1:g.67724861_67724872del	GRCh37
NC_000001.9:g.67497449_67497460del	NCBI36
NG_011498.1:g.97693_97704del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*50_*61del MANE Select	ENSP00000321345.5:n.*50_*61del
ENST00000347310.9:c.*50_*61del	ENSP00000321345.5:n.*50_*61del
ENST00000395227.2:c.*50_*61del	ENSP00000378652.2:n.*50_*61del
ENST00000425614.3:c.*50_*61del	ENSP00000387640.2:n.*50_*61del
ENST00000473881.2:c.*766_*777del	ENSP00000486667.1:n.*766_*777del
NM_144701.2:c.*50_*61del	NP_653302.2:n.*50_*61del
XM_005270516.2:c.*50_*61del	XP_005270573.1:n.*50_*61del
XM_011540789.1:c.*50_*61del	XP_011539091.1:n.*50_*61del
XM_011540790.1:c.*50_*61del	XP_011539092.1:n.*50_*61del
XM_011540791.1:c.*50_*61del	XP_011539093.1:n.*50_*61del
XM_011540790.3:c.*50_*61del	XP_011539092.1:n.*50_*61del
XM_011540791.3:c.*50_*61del	XP_011539093.1:n.*50_*61del
NM_144701.3:c.*50_*61del MANE Select	NP_653302.2:n.*50_*61del