Canonical Allele Identifier: CA1280066407

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113117979G= , CM000664.2:g.113117979G=	GRCh38
NC_000002.11:g.113875556G= , CM000664.1:g.113875556G=	GRCh37
NC_000002.10:g.113592027G=	NCBI36
NG_021240.1:g.5087G= , LRG_188:g.5087G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2087G=	ENSP00000387210.1:n.-272-2087G=
ENST00000465812.6:n.775+314G=
ENST00000696881.1:c.-322G=	ENSP00000512949.1:n.-322G=
ENST00000259206.9:c.-40G=	ENSP00000259206.5:n.-40G=
ENST00000354115.6:c.-40G=	ENSP00000329072.3:n.-40G=
ENST00000361779.7:c.-259G=	ENSP00000354816.3:n.-259G=
ENST00000409052.5:c.-272-2087G=	ENSP00000387210.1:n.-272-2087G=
NM_000577.4:c.-40G=	NP_000568.1:n.-40G=
NM_173841.2:c.-40G= , LRG_188t1:c.-40G=	NP_776213.1:n.-40G=
NM_173843.2:c.-259G=	NP_776215.1:n.-259G=
XM_006712497.2:c.-322G=	XP_006712560.1:n.-322G=
XM_011511121.1:c.-272-2087G=	XP_011509423.1:n.-272-2087G=
NM_001318914.1:c.-322G=	NP_001305843.1:n.-322G=
NM_000577.5:c.-40G=	NP_000568.1:n.-40G=
NM_001318914.2:c.-322G=	NP_001305843.1:n.-322G=
NM_173843.3:c.-259G=	NP_776215.1:n.-259G=
NM_173841.3:c.-40G=	NP_776213.1:n.-40G=