Canonical Allele Identifier: CA2509991938

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419471_102419472insTA , CM000664.2:g.102419471_102419472insTA	GRCh38
NC_000002.11:g.103035931_103035932insTA , CM000664.1:g.103035931_103035932insTA	GRCh37
NC_000002.10:g.102402363_102402364insTA	NCBI36
NG_011481.1:g.5678_5679insTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000264260.6:c.-337-90_-337-89insTA	ENSP00000264260.2:n.-337-90_-337-89insTA
ENST00000450855.1:c.-427_-426insTA	ENSP00000389815.1:n.-427_-426insTA
NM_003853.3:c.-337-90_-337-89insTA	NP_003844.1:n.-337-90_-337-89insTA
XM_011512087.1:c.-438-90_-438-89insTA	XP_011510389.1:n.-438-90_-438-89insTA
XM_011512087.2:c.-438-90_-438-89insTA	XP_011510389.1:n.-438-90_-438-89insTA
XM_024453197.1:c.-1292-90_-1292-89insTA	XP_024308965.1:n.-1292-90_-1292-89insTA
XM_024453198.1:c.-446-90_-446-89insTA	XP_024308966.1:n.-446-90_-446-89insTA
XM_024453199.1:c.-589-90_-589-89insTA	XP_024308967.1:n.-589-90_-589-89insTA
XM_024453201.1:c.-101+531_-101+532insTA	XP_024308969.1:n.-101+531_-101+532insTA
NM_001393486.1:c.-337-90_-337-89insTA	NP_001380415.1:n.-337-90_-337-89insTA
NM_001393488.1:c.-967-90_-967-89insTA	NP_001380417.1:n.-967-90_-967-89insTA
NM_001393489.1:c.-438-90_-438-89insTA	NP_001380418.1:n.-438-90_-438-89insTA
NM_003853.4:c.-337-90_-337-89insTA	NP_003844.1:n.-337-90_-337-89insTA