Canonical Allele Identifier: CA2000589119

Gene: IL18

Linked Data

• dbSNP Id: rs1866653839

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112162664_112162665insACACTGTACTACAGTTGGGTGTACACTGTAGT , CM000673.2:g.112162664_112162665insACACTGTACTACAGTTGGGTGTACACTGTAGT	GRCh38
NC_000011.9:g.112033387_112033388insACACTGTACTACAGTTGGGTGTACACTGTAGT , CM000673.1:g.112033387_112033388insACACTGTACTACAGTTGGGTGTACACTGTAGT	GRCh37
NC_000011.8:g.111538597_111538598insACACTGTACTACAGTTGGGTGTACACTGTAGT	NCBI36
NG_028143.1:g.6459_6460insGTGTACACCCAACTGTAGTACAGTGTACTACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280357.12:c.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA MANE Select	ENSP00000280357.7:n.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAG...
ENST00000280357.11:c.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	ENSP00000280357.7:n.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAG...
ENST00000524595.5:c.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	ENSP00000434561.1:n.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAG...
ENST00000525987.5:n.320-7755_320-7754insACACTGTACTACAGTTGGGTGTACACTGTAGT
ENST00000528832.1:c.-30+1247_-30+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	ENSP00000434161.1:n.-30+1247_-30+1248insGTGTACACCCAACTGTAGTAC...
ENST00000531744.5:c.315-7755_315-7754insACACTGTACTACAGTTGGGTGTACACTGTAGT	ENSP00000456957.1:n.315-7755_315-7754insACACTGTACTACAGTTGGGTG...
ENST00000532699.1:c.315-7755_315-7754insACACTGTACTACAGTTGGGTGTACACTGTAGT	ENSP00000456434.1:n.315-7755_315-7754insACACTGTACTACAGTTGGGTG...
ENST00000533858.5:n.191+1247_191+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA
ENST00000534225.1:n.188+1247_188+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA
NM_001243211.1:c.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	NP_001230140.1:n.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGT...
NM_001562.3:c.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	NP_001553.1:n.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGTACT...
XM_011542805.1:c.-30+1247_-30+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	XP_011541107.1:n.-30+1247_-30+1248insGTGTACACCCAACTGTAGTACAGT...
XM_011542806.1:c.-30+1247_-30+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	XP_011541108.1:n.-30+1247_-30+1248insGTGTACACCCAACTGTAGTACAGT...
XM_011542806.2:c.-30+1247_-30+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	XP_011541108.1:n.-30+1247_-30+1248insGTGTACACCCAACTGTAGTACAGT...
NM_001562.4:c.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA MANE Select	NP_001553.1:n.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGTACT...
NM_001243211.2:c.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	NP_001230140.1:n.-9+1247_-9+1248insGTGTACACCCAACTGTAGTACAGTGT...
NM_001386420.1:c.-30+1247_-30+1248insGTGTACACCCAACTGTAGTACAGTGTACTACA	NP_001373349.1:n.-30+1247_-30+1248insGTGTACACCCAACTGTAGTACAGT...