Canonical Allele Identifier: CA52939649

Gene: IL18R1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102397290G>T , CM000664.2:g.102397290G>T	GRCh38
NC_000002.11:g.103013750G>T , CM000664.1:g.103013750G>T	GRCh37
NC_000002.10:g.102380182G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233957.7:c.*404G>T MANE Select	ENSP00000233957.1:n.*404G>T
ENST00000677287.1:c.2087G>T	ENSP00000503023.1:n.2087G>T
ENST00000233957.5:c.*404G>T	ENSP00000233957.1:n.*404G>T
ENST00000409599.5:c.*404G>T	ENSP00000387211.1:n.*404G>T
NM_001282399.1:c.*404G>T	NP_001269328.1:n.*404G>T
NM_003855.3:c.*404G>T	NP_003846.1:n.*404G>T
XM_005264039.3:c.*404G>T	XP_005264096.1:n.*404G>T
XM_005264040.3:c.*404G>T	XP_005264097.1:n.*404G>T
XM_006712823.2:c.*404G>T	XP_006712886.1:n.*404G>T
XM_011512099.1:c.*404G>T	XP_011510401.1:n.*404G>T
XM_017005181.2:c.*404G>T	XP_016860670.1:n.*404G>T
XM_017005182.1:c.*404G>T	XP_016860671.1:n.*404G>T
XM_017005183.1:c.*404G>T	XP_016860672.1:n.*404G>T
XM_017005184.1:c.*404G>T	XP_016860673.1:n.*404G>T
XM_024453202.1:c.*404G>T	XP_024308970.1:n.*404G>T
XM_024453203.1:c.*404G>T	XP_024308971.1:n.*404G>T
XM_024453204.1:c.*404G>T	XP_024308972.1:n.*404G>T
XM_024453205.1:c.*404G>T	XP_024308973.1:n.*404G>T
NM_001282399.2:c.*404G>T	NP_001269328.1:n.*404G>T
NM_001371418.1:c.*404G>T	NP_001358347.1:n.*404G>T
NM_001371421.1:c.*404G>T	NP_001358350.1:n.*404G>T
NM_001371422.1:c.*404G>T	NP_001358351.1:n.*404G>T
NM_001371423.1:c.*404G>T	NP_001358352.1:n.*404G>T
NM_001371424.1:c.*404G>T	NP_001358353.1:n.*404G>T
NM_003855.5:c.*404G>T MANE Select	NP_003846.1:n.*404G>T