Canonical Allele Identifier: CA1280066429

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113118010G= , CM000664.2:g.113118010G=	GRCh38
NC_000002.11:g.113875587G= , CM000664.1:g.113875587G=	GRCh37
NC_000002.10:g.113592058G=	NCBI36
NG_021240.1:g.5118G= , LRG_188:g.5118G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2056G=	ENSP00000387210.1:n.-272-2056G=
ENST00000465812.6:n.775+345G=
ENST00000696881.1:c.-291G=	ENSP00000512949.1:n.-291G=
ENST00000259206.9:c.-9G=	ENSP00000259206.5:n.-9G=
ENST00000354115.6:c.-9G=	ENSP00000329072.3:n.-9G=
ENST00000361779.7:c.-228G=	ENSP00000354816.3:n.-228G=
ENST00000409052.5:c.-272-2056G=	ENSP00000387210.1:n.-272-2056G=
ENST00000486167.1:n.30G=
NM_000577.4:c.-9G=	NP_000568.1:n.-9G=
NM_173841.2:c.-9G= , LRG_188t1:c.-9G=	NP_776213.1:n.-9G=
NM_173843.2:c.-228G=	NP_776215.1:n.-228G=
XM_006712497.2:c.-291G=	XP_006712560.1:n.-291G=
XM_011511121.1:c.-272-2056G=	XP_011509423.1:n.-272-2056G=
NM_001318914.1:c.-291G=	NP_001305843.1:n.-291G=
NM_000577.5:c.-9G=	NP_000568.1:n.-9G=
NM_001318914.2:c.-291G=	NP_001305843.1:n.-291G=
NM_173843.3:c.-228G=	NP_776215.1:n.-228G=
NM_173841.3:c.-9G=	NP_776213.1:n.-9G=