Canonical Allele Identifier: CA1275204046
Gene: IL1RL1 HGNC NCBI
IL18R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102329152T= , CM000664.2:g.102329152T= GRCh38
NC_000002.11:g.102945612T= , CM000664.1:g.102945612T= GRCh37
NC_000002.10:g.102312044T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000233954.6:c.-149-8964T= (IL1RL1) MANE Select ENSP00000233954.1:n.-149-8964T=
ENST00000233954.5:c.-149-8964T= (IL1RL1) ENSP00000233954.1:n.-149-8964T=
ENST00000404917.6:c.-146-9829T= (IL1RL1) ENSP00000384822.2:n.-146-9829T=
ENST00000410040.5:c.-29+17529T= (IL18R1) ENSP00000386663.1:n.-29+17529T=
ENST00000447231.5:c.-149-8964T= (IL1RL1) ENSP00000409437.1:n.-149-8964T=
ENST00000473175.1:n.96-8964T= (IL1RL1)
NM_001282408.1:c.-146-9829T= (IL1RL1) NP_001269337.1:n.-146-9829T=
NM_016232.4:c.-149-8964T= (IL1RL1) NP_057316.3:n.-149-8964T=
XM_011512151.1:c.-149-8964T= (IL1RL1) XP_011510453.1:n.-149-8964T=
NM_016232.5:c.-149-8964T= (IL1RL1) MANE Select NP_057316.3:n.-149-8964T=
NM_001282408.2:c.-146-9829T= (IL1RL1) NP_001269337.1:n.-146-9829T=