Canonical Allele Identifier: CA1630855335

Gene: IL18

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112155980A= , CM000673.2:g.112155980A=	GRCh38
NC_000011.9:g.112026703A= , CM000673.1:g.112026703A=	GRCh37
NC_000011.8:g.111531913A=	NCBI36
NG_028143.1:g.13138T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001562.4:c.-8-919T= MANE Select	NP_001553.1:n.-8-919T=
ENST00000280357.12:c.-8-919T= MANE Select	ENSP00000280357.7:n.-8-919T=
NM_001243211.1:c.-8-919T=	NP_001230140.1:n.-8-919T=
NM_001243211.2:c.-8-919T=	NP_001230140.1:n.-8-919T=
NM_001386420.1:c.-29-898T=	NP_001373349.1:n.-29-898T=
NM_001562.3:c.-8-919T=	NP_001553.1:n.-8-919T=
ENST00000280357.11:c.-8-919T=	ENSP00000280357.7:n.-8-919T=
ENST00000524595.5:c.-8-919T=	ENSP00000434561.1:n.-8-919T=
ENST00000525987.5:n.320-14439A=
ENST00000528832.1:c.-29-898T=	ENSP00000434161.1:n.-29-898T=
ENST00000531744.5:c.315-14439A=	ENSP00000456957.1:n.315-14439A=
ENST00000532699.1:c.315-14439A=	ENSP00000456434.1:n.315-14439A=
ENST00000533858.5:n.192-919T=
ENST00000534225.1:n.189-919T=
XM_011542805.1:c.-29-898T=	XP_011541107.1:n.-29-898T=
XM_011542806.1:c.-29-898T=	XP_011541108.1:n.-29-898T=
XM_011542806.2:c.-29-898T=	XP_011541108.1:n.-29-898T=