Canonical Allele Identifier: CA2511990439

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419469_102419470insGTGGC , CM000664.2:g.102419469_102419470insGTGGC	GRCh38
NC_000002.11:g.103035929_103035930insGTGGC , CM000664.1:g.103035929_103035930insGTGGC	GRCh37
NC_000002.10:g.102402361_102402362insGTGGC	NCBI36
NG_011481.1:g.5676_5677insGTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-337-92_-337-91insGTGGC	ENSP00000264260.2:n.-337-92_-337-91insGTGGC
ENST00000450855.1:c.-429_-428insGTGGC	ENSP00000389815.1:n.-429_-428insGTGGC
NM_003853.3:c.-337-92_-337-91insGTGGC	NP_003844.1:n.-337-92_-337-91insGTGGC
XM_011512087.1:c.-438-92_-438-91insGTGGC	XP_011510389.1:n.-438-92_-438-91insGTGGC
XM_011512087.2:c.-438-92_-438-91insGTGGC	XP_011510389.1:n.-438-92_-438-91insGTGGC
XM_024453197.1:c.-1292-92_-1292-91insGTGGC	XP_024308965.1:n.-1292-92_-1292-91insGTGGC
XM_024453198.1:c.-446-92_-446-91insGTGGC	XP_024308966.1:n.-446-92_-446-91insGTGGC
XM_024453199.1:c.-589-92_-589-91insGTGGC	XP_024308967.1:n.-589-92_-589-91insGTGGC
XM_024453201.1:c.-101+529_-101+530insGTGGC	XP_024308969.1:n.-101+529_-101+530insGTGGC
NM_001393486.1:c.-337-92_-337-91insGTGGC	NP_001380415.1:n.-337-92_-337-91insGTGGC
NM_001393488.1:c.-967-92_-967-91insGTGGC	NP_001380417.1:n.-967-92_-967-91insGTGGC
NM_001393489.1:c.-438-92_-438-91insGTGGC	NP_001380418.1:n.-438-92_-438-91insGTGGC
NM_003853.4:c.-337-92_-337-91insGTGGC	NP_003844.1:n.-337-92_-337-91insGTGGC