Canonical Allele Identifier: CA1280073349

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132791G= , CM000664.2:g.113132791G=	GRCh38
NC_000002.11:g.113890368G= , CM000664.1:g.113890368G=	GRCh37
NC_000002.10:g.113606839G=	NCBI36
NG_021240.1:g.19899G= , LRG_188:g.19899G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.352G=	ENSP00000387210.1:p.Ala118=
ENST00000696879.1:c.352G=	ENSP00000512947.1:p.Ala118=
ENST00000696880.1:c.352G=	ENSP00000512948.1:p.Ala118=
ENST00000696881.1:c.352G=	ENSP00000512949.1:p.Ala118=
ENST00000696882.1:c.*224G=	ENSP00000512950.1:n.*224G=
ENST00000696883.1:n.399G=
ENST00000409930.4:c.454G= MANE Select	ENSP00000387173.3:p.Ala152=
ENST00000259206.9:c.463G=	ENSP00000259206.5:p.Ala155=
ENST00000354115.6:c.400G=	ENSP00000329072.3:p.Ala134=
ENST00000361779.7:c.352G=	ENSP00000354816.3:p.Ala118=
ENST00000409052.5:c.352G=	ENSP00000387210.1:p.Ala118=
ENST00000409930.3:c.454G=	ENSP00000387173.3:p.Ala152=
NM_000577.4:c.400G=	NP_000568.1:p.Ala134=
NM_173841.2:c.463G= , LRG_188t1:c.463G=	NP_776213.1:p.Ala155=
NM_173842.2:c.454G=	NP_776214.1:p.Ala152=
NM_173843.2:c.352G=	NP_776215.1:p.Ala118=
XM_005263661.3:c.352G=	XP_005263718.1:p.Ala118=
XM_006712497.2:c.352G=	XP_006712560.1:p.Ala118=
XM_011511121.1:c.352G=	XP_011509423.1:p.Ala118=
NM_001318914.1:c.352G=	NP_001305843.1:p.Ala118=
XM_005263661.4:c.352G=	XP_005263718.1:p.Ala118=
NM_000577.5:c.400G=	NP_000568.1:p.Ala134=
NM_001318914.2:c.352G=	NP_001305843.1:p.Ala118=
NM_173842.3:c.454G= MANE Select	NP_776214.1:p.Ala152=
NM_173843.3:c.352G=	NP_776215.1:p.Ala118=
NM_001379360.1:c.352G=	NP_001366289.1:p.Ala118=
NM_173841.3:c.463G=	NP_776213.1:p.Ala155=