Canonical Allele Identifier: CA2660478178

Gene: IL18RAP

Linked Data

• gnomAD v4: 2-102419498-C-CTCTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419502_102419503insATCTC , CM000664.2:g.102419502_102419503insATCTC	GRCh38
NC_000002.11:g.103035962_103035963insATCTC , CM000664.1:g.103035962_103035963insATCTC	GRCh37
NC_000002.10:g.102402394_102402395insATCTC	NCBI36
NG_011481.1:g.5709_5710insATCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-337-59_-337-58insATCTC	ENSP00000264260.2:n.-337-59_-337-58insATCTC
ENST00000450855.1:c.-396_-395insATCTC	ENSP00000389815.1:n.-396_-395insATCTC
NM_003853.3:c.-337-59_-337-58insATCTC	NP_003844.1:n.-337-59_-337-58insATCTC
XM_011512087.1:c.-438-59_-438-58insATCTC	XP_011510389.1:n.-438-59_-438-58insATCTC
XM_011512087.2:c.-438-59_-438-58insATCTC	XP_011510389.1:n.-438-59_-438-58insATCTC
XM_024453197.1:c.-1292-59_-1292-58insATCTC	XP_024308965.1:n.-1292-59_-1292-58insATCTC
XM_024453198.1:c.-446-59_-446-58insATCTC	XP_024308966.1:n.-446-59_-446-58insATCTC
XM_024453199.1:c.-589-59_-589-58insATCTC	XP_024308967.1:n.-589-59_-589-58insATCTC
XM_024453201.1:c.-101+562_-101+563insATCTC	XP_024308969.1:n.-101+562_-101+563insATCTC
NM_001393486.1:c.-337-59_-337-58insATCTC	NP_001380415.1:n.-337-59_-337-58insATCTC
NM_001393488.1:c.-967-59_-967-58insATCTC	NP_001380417.1:n.-967-59_-967-58insATCTC
NM_001393489.1:c.-438-59_-438-58insATCTC	NP_001380418.1:n.-438-59_-438-58insATCTC
NM_003853.4:c.-337-59_-337-58insATCTC	NP_003844.1:n.-337-59_-337-58insATCTC