Canonical Allele Identifier: CA2523723160

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419464_102419465insGCT , CM000664.2:g.102419464_102419465insGCT	GRCh38
NC_000002.11:g.103035924_103035925insGCT , CM000664.1:g.103035924_103035925insGCT	GRCh37
NC_000002.10:g.102402356_102402357insGCT	NCBI36
NG_011481.1:g.5671_5672insGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-337-97_-337-96insGCT	ENSP00000264260.2:n.-337-97_-337-96insGCT
ENST00000450855.1:c.-434_-433insGCT	ENSP00000389815.1:n.-434_-433insGCT
NM_003853.3:c.-337-97_-337-96insGCT	NP_003844.1:n.-337-97_-337-96insGCT
XM_011512087.1:c.-438-97_-438-96insGCT	XP_011510389.1:n.-438-97_-438-96insGCT
XM_011512087.2:c.-438-97_-438-96insGCT	XP_011510389.1:n.-438-97_-438-96insGCT
XM_024453197.1:c.-1292-97_-1292-96insGCT	XP_024308965.1:n.-1292-97_-1292-96insGCT
XM_024453198.1:c.-446-97_-446-96insGCT	XP_024308966.1:n.-446-97_-446-96insGCT
XM_024453199.1:c.-589-97_-589-96insGCT	XP_024308967.1:n.-589-97_-589-96insGCT
XM_024453201.1:c.-101+524_-101+525insGCT	XP_024308969.1:n.-101+524_-101+525insGCT
NM_001393486.1:c.-337-97_-337-96insGCT	NP_001380415.1:n.-337-97_-337-96insGCT
NM_001393488.1:c.-967-97_-967-96insGCT	NP_001380417.1:n.-967-97_-967-96insGCT
NM_001393489.1:c.-438-97_-438-96insGCT	NP_001380418.1:n.-438-97_-438-96insGCT
NM_003853.4:c.-337-97_-337-96insGCT	NP_003844.1:n.-337-97_-337-96insGCT