Canonical Allele Identifier: CA1275216752
Gene: IL1RL1 HGNC NCBI
IL18R1 HGNC NCBI

Linked Data

dbSNP Id: rs112164401

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102341183_102341184insTTTTTTTTTTTTTTTTTTTTTTTT , CM000664.2:g.102341183_102341184insTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000002.11:g.102957643_102957644insTTTTTTTTTTTTTTTTTTTTTTTT , CM000664.1:g.102957643_102957644insTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000002.10:g.102324075_102324076insTTTTTTTTTTTTTTTTTTTTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000233954.6:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) MANE Select ENSP00000233954.1:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000233954.5:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) ENSP00000233954.1:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000311734.6:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) ENSP00000310371.2:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000404917.6:c.259+355_259+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) ENSP00000384822.2:n.259+355_259+356insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000409584.5:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) ENSP00000386618.1:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000410040.5:c.-28-21450_-28-21449insTTTTTTTTTTTTTTTTTTTTTTTT (IL18R1) ENSP00000386663.1:n.-28-21450_-28-21449insTTTTTTTTTTTTTTTTTTT...
ENST00000427077.1:c.611-5_611-4insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) ENSP00000391120.1:n.611-5_611-4insTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000482701.5:n.443+911_443+912insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1)
NM_001282408.1:c.259+355_259+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) NP_001269337.1:n.259+355_259+356insTTTTTTTTTTTTTTTTTTTTTTTT
NM_003856.3:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) NP_003847.2:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT
NM_016232.4:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) NP_057316.3:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT
NR_104167.1:n.848-5_848-4insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1)
XM_006712839.2:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) XP_006712902.1:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT
XM_011512151.1:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) XP_011510453.1:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT
XM_006712839.3:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) XP_006712902.1:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT
NM_003856.4:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) NP_003847.2:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT
NM_016232.5:c.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) MANE Select NP_057316.3:n.610+355_610+356insTTTTTTTTTTTTTTTTTTTTTTTT
NR_104167.2:n.841-5_841-4insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1)
NM_001282408.2:c.259+355_259+356insTTTTTTTTTTTTTTTTTTTTTTTT (IL1RL1) NP_001269337.1:n.259+355_259+356insTTTTTTTTTTTTTTTTTTTTTTTT