Canonical Allele Identifier: CA1275255109

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419386_102419390delinsCTCTG , CM000664.2:g.102419386_102419390delinsCTCTG	GRCh38
NC_000002.11:g.103035846_103035850delinsCTCTG , CM000664.1:g.103035846_103035850delinsCTCTG	GRCh37
NC_000002.10:g.102402278_102402282delinsCTCTG	NCBI36
NG_011481.1:g.5593_5597delinsCTCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000264260.6:c.-337-175_-337-171delinsCTCTG	ENSP00000264260.2:n.-337-175_-337-171delinsCTCTG
NM_003853.3:c.-337-175_-337-171delinsCTCTG	NP_003844.1:n.-337-175_-337-171delinsCTCTG
XM_011512087.1:c.-438-175_-438-171delinsCTCTG	XP_011510389.1:n.-438-175_-438-171delinsCTCTG
XM_011512087.2:c.-438-175_-438-171delinsCTCTG	XP_011510389.1:n.-438-175_-438-171delinsCTCTG
XM_024453197.1:c.-1292-175_-1292-171delinsCTCTG	XP_024308965.1:n.-1292-175_-1292-171delinsCTCTG
XM_024453198.1:c.-446-175_-446-171delinsCTCTG	XP_024308966.1:n.-446-175_-446-171delinsCTCTG
XM_024453199.1:c.-589-175_-589-171delinsCTCTG	XP_024308967.1:n.-589-175_-589-171delinsCTCTG
XM_024453201.1:c.-101+446_-101+450delinsCTCTG	XP_024308969.1:n.-101+446_-101+450delinsCTCTG
NM_001393486.1:c.-337-175_-337-171delinsCTCTG	NP_001380415.1:n.-337-175_-337-171delinsCTCTG
NM_001393488.1:c.-967-175_-967-171delinsCTCTG	NP_001380417.1:n.-967-175_-967-171delinsCTCTG
NM_001393489.1:c.-438-175_-438-171delinsCTCTG	NP_001380418.1:n.-438-175_-438-171delinsCTCTG
NM_003853.4:c.-337-175_-337-171delinsCTCTG	NP_003844.1:n.-337-175_-337-171delinsCTCTG