Canonical Allele Identifier: CA1275255102

Gene: IL18RAP

Linked Data

• dbSNP Id: rs1681433212

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419382_102419386del , CM000664.2:g.102419382_102419386del	GRCh38
NC_000002.11:g.103035842_103035846del , CM000664.1:g.103035842_103035846del	GRCh37
NC_000002.10:g.102402274_102402278del	NCBI36
NG_011481.1:g.5589_5593del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-337-179_-337-175del	ENSP00000264260.2:n.-337-179_-337-175del
NM_003853.3:c.-337-179_-337-175del	NP_003844.1:n.-337-179_-337-175del
XM_011512087.1:c.-438-179_-438-175del	XP_011510389.1:n.-438-179_-438-175del
XM_011512087.2:c.-438-179_-438-175del	XP_011510389.1:n.-438-179_-438-175del
XM_024453197.1:c.-1292-179_-1292-175del	XP_024308965.1:n.-1292-179_-1292-175del
XM_024453198.1:c.-446-179_-446-175del	XP_024308966.1:n.-446-179_-446-175del
XM_024453199.1:c.-589-179_-589-175del	XP_024308967.1:n.-589-179_-589-175del
XM_024453201.1:c.-101+442_-101+446del	XP_024308969.1:n.-101+442_-101+446del
NM_001393486.1:c.-337-179_-337-175del	NP_001380415.1:n.-337-179_-337-175del
NM_001393488.1:c.-967-179_-967-175del	NP_001380417.1:n.-967-179_-967-175del
NM_001393489.1:c.-438-179_-438-175del	NP_001380418.1:n.-438-179_-438-175del
NM_003853.4:c.-337-179_-337-175del	NP_003844.1:n.-337-179_-337-175del