Canonical Allele Identifier: CA2660480995

Gene: IL18RAP

Linked Data

• gnomAD v4: 2-102452237-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102452237A>G , CM000664.2:g.102452237A>G	GRCh38
NC_000002.11:g.103068697A>G , CM000664.1:g.103068697A>G	GRCh37
NC_000002.10:g.102435129A>G	NCBI36
NG_011481.1:g.38444A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000687160.1:c.*56A>G MANE Select	ENSP00000510345.1:n.*56A>G
ENST00000264260.6:c.*56A>G	ENSP00000264260.2:n.*56A>G
ENST00000409369.1:c.*56A>G	ENSP00000387201.1:n.*56A>G
NM_003853.3:c.*56A>G	NP_003844.1:n.*56A>G
XM_011512087.1:c.*56A>G	XP_011510389.1:n.*56A>G
XM_011512088.1:c.*56A>G	XP_011510390.1:n.*56A>G
XM_011512087.2:c.*56A>G	XP_011510389.1:n.*56A>G
XM_011512088.2:c.*56A>G	XP_011510390.1:n.*56A>G
XM_017005173.1:c.*56A>G	XP_016860662.1:n.*56A>G
XM_024453197.1:c.*56A>G	XP_024308965.1:n.*56A>G
XM_024453198.1:c.*56A>G	XP_024308966.1:n.*56A>G
XM_024453199.1:c.*56A>G	XP_024308967.1:n.*56A>G
XM_024453200.1:c.*56A>G	XP_024308968.1:n.*56A>G
XM_024453201.1:c.*56A>G	XP_024308969.1:n.*56A>G
NM_001393486.1:c.*56A>G	NP_001380415.1:n.*56A>G
NM_001393487.1:c.*56A>G MANE Select	NP_001380416.1:n.*56A>G
NM_001393488.1:c.*56A>G	NP_001380417.1:n.*56A>G
NM_001393489.1:c.*56A>G	NP_001380418.1:n.*56A>G
NM_003853.4:c.*56A>G	NP_003844.1:n.*56A>G