Canonical Allele Identifier: CA2503055400

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419443_102419450del , CM000664.2:g.102419443_102419450del	GRCh38
NC_000002.11:g.103035903_103035910del , CM000664.1:g.103035903_103035910del	GRCh37
NC_000002.10:g.102402335_102402342del	NCBI36
NG_011481.1:g.5650_5657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-337-118_-337-111del	ENSP00000264260.2:n.-337-118_-337-111del
NM_003853.3:c.-337-118_-337-111del	NP_003844.1:n.-337-118_-337-111del
XM_011512087.1:c.-438-118_-438-111del	XP_011510389.1:n.-438-118_-438-111del
XM_011512087.2:c.-438-118_-438-111del	XP_011510389.1:n.-438-118_-438-111del
XM_024453197.1:c.-1292-118_-1292-111del	XP_024308965.1:n.-1292-118_-1292-111del
XM_024453198.1:c.-446-118_-446-111del	XP_024308966.1:n.-446-118_-446-111del
XM_024453199.1:c.-589-118_-589-111del	XP_024308967.1:n.-589-118_-589-111del
XM_024453201.1:c.-101+503_-101+510del	XP_024308969.1:n.-101+503_-101+510del
NM_001393486.1:c.-337-118_-337-111del	NP_001380415.1:n.-337-118_-337-111del
NM_001393488.1:c.-967-118_-967-111del	NP_001380417.1:n.-967-118_-967-111del
NM_001393489.1:c.-438-118_-438-111del	NP_001380418.1:n.-438-118_-438-111del
NM_003853.4:c.-337-118_-337-111del	NP_003844.1:n.-337-118_-337-111del