Canonical Allele Identifier: CA2739768859

Gene: IL1RL1 IL18R1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102341260T>A , CM000664.2:g.102341260T>A	GRCh38
NC_000002.11:g.102957720T>A , CM000664.1:g.102957720T>A	GRCh37
NC_000002.10:g.102324152T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233954.6:c.610+432T>A (IL1RL1) MANE Select	ENSP00000233954.1:n.610+432T>A
ENST00000233954.5:c.610+432T>A (IL1RL1)	ENSP00000233954.1:n.610+432T>A
ENST00000311734.6:c.610+432T>A (IL1RL1)	ENSP00000310371.2:n.610+432T>A
ENST00000404917.6:c.259+432T>A (IL1RL1)	ENSP00000384822.2:n.259+432T>A
ENST00000409584.5:c.610+432T>A (IL1RL1)	ENSP00000386618.1:n.610+432T>A
ENST00000410040.5:c.-28-21373T>A (IL18R1)	ENSP00000386663.1:n.-28-21373T>A
ENST00000427077.1:c.683T>A (IL1RL1)	ENSP00000391120.1:p.Met228Lys
ENST00000482701.5:n.444-963T>A (IL1RL1)
NM_001282408.1:c.259+432T>A (IL1RL1)	NP_001269337.1:n.259+432T>A
NM_003856.3:c.610+432T>A (IL1RL1)	NP_003847.2:n.610+432T>A
NM_016232.4:c.610+432T>A (IL1RL1)	NP_057316.3:n.610+432T>A
NR_104167.1:n.920T>A (IL1RL1)
XM_006712839.2:c.610+432T>A (IL1RL1)	XP_006712902.1:n.610+432T>A
XM_011512151.1:c.610+432T>A (IL1RL1)	XP_011510453.1:n.610+432T>A
XM_006712839.3:c.610+432T>A (IL1RL1)	XP_006712902.1:n.610+432T>A
NM_003856.4:c.610+432T>A (IL1RL1)	NP_003847.2:n.610+432T>A
NM_016232.5:c.610+432T>A (IL1RL1) MANE Select	NP_057316.3:n.610+432T>A
NR_104167.2:n.913T>A (IL1RL1)
NM_001282408.2:c.259+432T>A (IL1RL1)	NP_001269337.1:n.259+432T>A