Canonical Allele Identifier: CA2751471622
Gene: IL1RL1 HGNC NCBI
IL18R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102341166_102341167del , CM000664.2:g.102341166_102341167del GRCh38
NC_000002.11:g.102957626_102957627del , CM000664.1:g.102957626_102957627del GRCh37
NC_000002.10:g.102324058_102324059del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000233954.6:c.610+338_610+339del (IL1RL1) MANE Select ENSP00000233954.1:n.610+338_610+339del
ENST00000233954.5:c.610+338_610+339del (IL1RL1) ENSP00000233954.1:n.610+338_610+339del
ENST00000311734.6:c.610+338_610+339del (IL1RL1) ENSP00000310371.2:n.610+338_610+339del
ENST00000404917.6:c.259+338_259+339del (IL1RL1) ENSP00000384822.2:n.259+338_259+339del
ENST00000409584.5:c.610+338_610+339del (IL1RL1) ENSP00000386618.1:n.610+338_610+339del
ENST00000410040.5:c.-28-21467_-28-21466del (IL18R1) ENSP00000386663.1:n.-28-21467_-28-21466del
ENST00000427077.1:c.611-22_611-21del (IL1RL1) ENSP00000391120.1:n.611-22_611-21del
ENST00000482701.5:n.443+894_443+895del (IL1RL1)
NM_001282408.1:c.259+338_259+339del (IL1RL1) NP_001269337.1:n.259+338_259+339del
NM_003856.3:c.610+338_610+339del (IL1RL1) NP_003847.2:n.610+338_610+339del
NM_016232.4:c.610+338_610+339del (IL1RL1) NP_057316.3:n.610+338_610+339del
NR_104167.1:n.848-22_848-21del (IL1RL1)
XM_006712839.2:c.610+338_610+339del (IL1RL1) XP_006712902.1:n.610+338_610+339del
XM_011512151.1:c.610+338_610+339del (IL1RL1) XP_011510453.1:n.610+338_610+339del
XM_006712839.3:c.610+338_610+339del (IL1RL1) XP_006712902.1:n.610+338_610+339del
NM_003856.4:c.610+338_610+339del (IL1RL1) NP_003847.2:n.610+338_610+339del
NM_016232.5:c.610+338_610+339del (IL1RL1) MANE Select NP_057316.3:n.610+338_610+339del
NR_104167.2:n.841-22_841-21del (IL1RL1)
NM_001282408.2:c.259+338_259+339del (IL1RL1) NP_001269337.1:n.259+338_259+339del