Canonical Allele Identifier: CA2000589139

Gene: IL18

Linked Data

• dbSNP Id: rs1866654642

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112162704_112162706del , CM000673.2:g.112162704_112162706del	GRCh38
NC_000011.9:g.112033427_112033429del , CM000673.1:g.112033427_112033429del	GRCh37
NC_000011.8:g.111538637_111538639del	NCBI36
NG_028143.1:g.6413_6415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280357.12:c.-9+1201_-9+1203del MANE Select	ENSP00000280357.7:n.-9+1201_-9+1203del
ENST00000280357.11:c.-9+1201_-9+1203del	ENSP00000280357.7:n.-9+1201_-9+1203del
ENST00000524595.5:c.-9+1201_-9+1203del	ENSP00000434561.1:n.-9+1201_-9+1203del
ENST00000525987.5:n.320-7715_320-7713del
ENST00000528832.1:c.-30+1201_-30+1203del	ENSP00000434161.1:n.-30+1201_-30+1203del
ENST00000531744.5:c.315-7715_315-7713del	ENSP00000456957.1:n.315-7715_315-7713del
ENST00000532699.1:c.315-7715_315-7713del	ENSP00000456434.1:n.315-7715_315-7713del
ENST00000533858.5:n.191+1201_191+1203del
ENST00000534225.1:n.188+1201_188+1203del
NM_001243211.1:c.-9+1201_-9+1203del	NP_001230140.1:n.-9+1201_-9+1203del
NM_001562.3:c.-9+1201_-9+1203del	NP_001553.1:n.-9+1201_-9+1203del
XM_011542805.1:c.-30+1201_-30+1203del	XP_011541107.1:n.-30+1201_-30+1203del
XM_011542806.1:c.-30+1201_-30+1203del	XP_011541108.1:n.-30+1201_-30+1203del
XM_011542806.2:c.-30+1201_-30+1203del	XP_011541108.1:n.-30+1201_-30+1203del
NM_001562.4:c.-9+1201_-9+1203del MANE Select	NP_001553.1:n.-9+1201_-9+1203del
NM_001243211.2:c.-9+1201_-9+1203del	NP_001230140.1:n.-9+1201_-9+1203del
NM_001386420.1:c.-30+1201_-30+1203del	NP_001373349.1:n.-30+1201_-30+1203del