Canonical Allele Identifier: CA1280073377

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132866G= , CM000664.2:g.113132866G=	GRCh38
NC_000002.11:g.113890443G= , CM000664.1:g.113890443G=	GRCh37
NC_000002.10:g.113606914G=	NCBI36
NG_021240.1:g.19974G= , LRG_188:g.19974G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.427G=	ENSP00000387210.1:p.Glu143=
ENST00000696879.1:c.427G=	ENSP00000512947.1:p.Glu143=
ENST00000696880.1:c.427G=	ENSP00000512948.1:p.Glu143=
ENST00000696881.1:c.427G=	ENSP00000512949.1:p.Glu143=
ENST00000696882.1:c.*299G=	ENSP00000512950.1:n.*299G=
ENST00000696883.1:n.474G=
ENST00000409930.4:c.529G= MANE Select	ENSP00000387173.3:p.Glu177=
ENST00000259206.9:c.538G=	ENSP00000259206.5:p.Glu180=
ENST00000354115.6:c.475G=	ENSP00000329072.3:p.Glu159=
ENST00000361779.7:c.427G=	ENSP00000354816.3:p.Glu143=
ENST00000409052.5:c.427G=	ENSP00000387210.1:p.Glu143=
ENST00000409930.3:c.529G=	ENSP00000387173.3:p.Glu177=
NM_000577.4:c.475G=	NP_000568.1:p.Glu159=
NM_173841.2:c.538G= , LRG_188t1:c.538G=	NP_776213.1:p.Glu180=
NM_173842.2:c.529G=	NP_776214.1:p.Glu177=
NM_173843.2:c.427G=	NP_776215.1:p.Glu143=
XM_005263661.3:c.427G=	XP_005263718.1:p.Glu143=
XM_006712497.2:c.427G=	XP_006712560.1:p.Glu143=
XM_011511121.1:c.427G=	XP_011509423.1:p.Glu143=
NM_001318914.1:c.427G=	NP_001305843.1:p.Glu143=
XM_005263661.4:c.427G=	XP_005263718.1:p.Glu143=
NM_000577.5:c.475G=	NP_000568.1:p.Glu159=
NM_001318914.2:c.427G=	NP_001305843.1:p.Glu143=
NM_173842.3:c.529G= MANE Select	NP_776214.1:p.Glu177=
NM_173843.3:c.427G=	NP_776215.1:p.Glu143=
NM_001379360.1:c.427G=	NP_001366289.1:p.Glu143=
NM_173841.3:c.538G=	NP_776213.1:p.Glu180=