Canonical Allele Identifier: CA1280073607

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133310T= , CM000664.2:g.113133310T=	GRCh38
NC_000002.11:g.113890887T= , CM000664.1:g.113890887T=	GRCh37
NC_000002.10:g.113607358T=	NCBI36
NG_021240.1:g.20418T= , LRG_188:g.20418T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*439T=	ENSP00000387210.1:n.*439T=
ENST00000696879.1:c.*439T=	ENSP00000512947.1:n.*439T=
ENST00000696880.1:c.*212-55T=	ENSP00000512948.1:n.*212-55T=
ENST00000696882.1:c.*743T=	ENSP00000512950.1:n.*743T=
ENST00000409930.4:c.*439T= MANE Select	ENSP00000387173.3:n.*439T=
ENST00000259206.9:c.*439T=	ENSP00000259206.5:n.*439T=
ENST00000354115.6:c.*439T=	ENSP00000329072.3:n.*439T=
ENST00000361779.7:c.*439T=	ENSP00000354816.3:n.*439T=
ENST00000409052.5:c.*439T=	ENSP00000387210.1:n.*439T=
NM_000577.4:c.*439T=	NP_000568.1:n.*439T=
NM_173841.2:c.*439T= , LRG_188t1:c.*439T=	NP_776213.1:n.*439T=
NM_173842.2:c.*439T=	NP_776214.1:n.*439T=
NM_173843.2:c.*439T=	NP_776215.1:n.*439T=
XM_005263661.3:c.*439T=	XP_005263718.1:n.*439T=
XM_006712497.2:c.*439T=	XP_006712560.1:n.*439T=
XM_011511121.1:c.*439T=	XP_011509423.1:n.*439T=
NM_001318914.1:c.*439T=	NP_001305843.1:n.*439T=
XM_005263661.4:c.*439T=	XP_005263718.1:n.*439T=
NM_000577.5:c.*439T=	NP_000568.1:n.*439T=
NM_001318914.2:c.*439T=	NP_001305843.1:n.*439T=
NM_173842.3:c.*439T= MANE Select	NP_776214.1:n.*439T=
NM_173843.3:c.*439T=	NP_776215.1:n.*439T=
NM_001379360.1:c.*439T=	NP_001366289.1:n.*439T=
NM_173841.3:c.*439T=	NP_776213.1:n.*439T=