Canonical Allele Identifier: CA1275255101

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419380_102419385delinsCCAAAT , CM000664.2:g.102419380_102419385delinsCCAAAT	GRCh38
NC_000002.11:g.103035840_103035845delinsCCAAAT , CM000664.1:g.103035840_103035845delinsCCAAAT	GRCh37
NC_000002.10:g.102402272_102402277delinsCCAAAT	NCBI36
NG_011481.1:g.5587_5592delinsCCAAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000264260.6:c.-337-181_-337-176delinsCCAAAT	ENSP00000264260.2:n.-337-181_-337-176delinsCCAAAT
NM_003853.3:c.-337-181_-337-176delinsCCAAAT	NP_003844.1:n.-337-181_-337-176delinsCCAAAT
XM_011512087.1:c.-438-181_-438-176delinsCCAAAT	XP_011510389.1:n.-438-181_-438-176delinsCCAAAT
XM_011512087.2:c.-438-181_-438-176delinsCCAAAT	XP_011510389.1:n.-438-181_-438-176delinsCCAAAT
XM_024453197.1:c.-1292-181_-1292-176delinsCCAAAT	XP_024308965.1:n.-1292-181_-1292-176delinsCCAAAT
XM_024453198.1:c.-446-181_-446-176delinsCCAAAT	XP_024308966.1:n.-446-181_-446-176delinsCCAAAT
XM_024453199.1:c.-589-181_-589-176delinsCCAAAT	XP_024308967.1:n.-589-181_-589-176delinsCCAAAT
XM_024453201.1:c.-101+440_-101+445delinsCCAAAT	XP_024308969.1:n.-101+440_-101+445delinsCCAAAT
NM_001393486.1:c.-337-181_-337-176delinsCCAAAT	NP_001380415.1:n.-337-181_-337-176delinsCCAAAT
NM_001393488.1:c.-967-181_-967-176delinsCCAAAT	NP_001380417.1:n.-967-181_-967-176delinsCCAAAT
NM_001393489.1:c.-438-181_-438-176delinsCCAAAT	NP_001380418.1:n.-438-181_-438-176delinsCCAAAT
NM_003853.4:c.-337-181_-337-176delinsCCAAAT	NP_003844.1:n.-337-181_-337-176delinsCCAAAT