Canonical Allele Identifier: CA1280073239

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132522_113132523delinsCT , CM000664.2:g.113132522_113132523delinsCT	GRCh38
NC_000002.11:g.113890099_113890100delinsCT , CM000664.1:g.113890099_113890100delinsCT	GRCh37
NC_000002.10:g.113606570_113606571delinsCT	NCBI36
NG_021240.1:g.19630_19631delinsCT , LRG_188:g.19630_19631delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.217-134_217-133delinsCT	ENSP00000387210.1:n.217-134_217-133delinsCT
ENST00000696879.1:c.217-134_217-133delinsCT	ENSP00000512947.1:n.217-134_217-133delinsCT
ENST00000696880.1:c.217-134_217-133delinsCT	ENSP00000512948.1:n.217-134_217-133delinsCT
ENST00000696881.1:c.217-134_217-133delinsCT	ENSP00000512949.1:n.217-134_217-133delinsCT
ENST00000696882.1:c.*89-134_*89-133delinsCT	ENSP00000512950.1:n.*89-134_*89-133delinsCT
ENST00000696883.1:n.264-134_264-133delinsCT
ENST00000409930.4:c.319-134_319-133delinsCT MANE Select	ENSP00000387173.3:n.319-134_319-133delinsCT
ENST00000259206.9:c.328-134_328-133delinsCT	ENSP00000259206.5:n.328-134_328-133delinsCT
ENST00000354115.6:c.265-134_265-133delinsCT	ENSP00000329072.3:n.265-134_265-133delinsCT
ENST00000361779.7:c.217-134_217-133delinsCT	ENSP00000354816.3:n.217-134_217-133delinsCT
ENST00000409052.5:c.217-134_217-133delinsCT	ENSP00000387210.1:n.217-134_217-133delinsCT
ENST00000409930.3:c.319-134_319-133delinsCT	ENSP00000387173.3:n.319-134_319-133delinsCT
NM_000577.4:c.265-134_265-133delinsCT	NP_000568.1:n.265-134_265-133delinsCT
NM_173841.2:c.328-134_328-133delinsCT , LRG_188t1:c.328-134_328-133delinsCT	NP_776213.1:n.328-134_328-133delinsCT
NM_173842.2:c.319-134_319-133delinsCT	NP_776214.1:n.319-134_319-133delinsCT
NM_173843.2:c.217-134_217-133delinsCT	NP_776215.1:n.217-134_217-133delinsCT
XM_005263661.3:c.217-134_217-133delinsCT	XP_005263718.1:n.217-134_217-133delinsCT
XM_006712497.2:c.217-134_217-133delinsCT	XP_006712560.1:n.217-134_217-133delinsCT
XM_011511121.1:c.217-134_217-133delinsCT	XP_011509423.1:n.217-134_217-133delinsCT
NM_001318914.1:c.217-134_217-133delinsCT	NP_001305843.1:n.217-134_217-133delinsCT
XM_005263661.4:c.217-134_217-133delinsCT	XP_005263718.1:n.217-134_217-133delinsCT
NM_000577.5:c.265-134_265-133delinsCT	NP_000568.1:n.265-134_265-133delinsCT
NM_001318914.2:c.217-134_217-133delinsCT	NP_001305843.1:n.217-134_217-133delinsCT
NM_173842.3:c.319-134_319-133delinsCT MANE Select	NP_776214.1:n.319-134_319-133delinsCT
NM_173843.3:c.217-134_217-133delinsCT	NP_776215.1:n.217-134_217-133delinsCT
NM_001379360.1:c.217-134_217-133delinsCT	NP_001366289.1:n.217-134_217-133delinsCT
NM_173841.3:c.328-134_328-133delinsCT	NP_776213.1:n.328-134_328-133delinsCT