Canonical Allele Identifier: CA2660469865
Gene: IL1RL1 HGNC NCBI
IL18R1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102344382del , CM000664.2:g.102344382del GRCh38
NC_000002.11:g.102960842del , CM000664.1:g.102960842del GRCh37
NC_000002.10:g.102327274del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000233954.6:c.970+967del (IL1RL1) MANE Select ENSP00000233954.1:n.970+967del
ENST00000233954.5:c.970+967del (IL1RL1) ENSP00000233954.1:n.970+967del
ENST00000311734.6:c.*950del (IL1RL1) ENSP00000310371.2:n.*950del
ENST00000404917.6:c.*950del (IL1RL1) ENSP00000384822.2:n.*950del
ENST00000409584.5:c.*950del (IL1RL1) ENSP00000386618.1:n.*950del
ENST00000410040.5:c.-28-18251del (IL18R1) ENSP00000386663.1:n.-28-18251del
NM_001282408.1:c.*950del (IL1RL1) NP_001269337.1:n.*950del
NM_003856.3:c.*950del (IL1RL1) NP_003847.2:n.*950del
NM_016232.4:c.970+967del (IL1RL1) NP_057316.3:n.970+967del
NR_104167.1:n.2344del (IL1RL1)
XM_006712839.2:c.970+967del (IL1RL1) XP_006712902.1:n.970+967del
XM_011512151.1:c.*950del (IL1RL1) XP_011510453.1:n.*950del
XM_006712839.3:c.970+967del (IL1RL1) XP_006712902.1:n.970+967del
NM_003856.4:c.*950del (IL1RL1) NP_003847.2:n.*950del
NM_016232.5:c.970+967del (IL1RL1) MANE Select NP_057316.3:n.970+967del
NR_104167.2:n.2337del (IL1RL1)
NM_001282408.2:c.*950del (IL1RL1) NP_001269337.1:n.*950del