Canonical Allele Identifier: CA1280073343

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132770T= , CM000664.2:g.113132770T=	GRCh38
NC_000002.11:g.113890347T= , CM000664.1:g.113890347T=	GRCh37
NC_000002.10:g.113606818T=	NCBI36
NG_021240.1:g.19878T= , LRG_188:g.19878T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.331T=	ENSP00000387210.1:p.Phe111=
ENST00000696879.1:c.331T=	ENSP00000512947.1:p.Phe111=
ENST00000696880.1:c.331T=	ENSP00000512948.1:p.Phe111=
ENST00000696881.1:c.331T=	ENSP00000512949.1:p.Phe111=
ENST00000696882.1:c.*203T=	ENSP00000512950.1:n.*203T=
ENST00000696883.1:n.378T=
ENST00000409930.4:c.433T= MANE Select	ENSP00000387173.3:p.Phe145=
ENST00000259206.9:c.442T=	ENSP00000259206.5:p.Phe148=
ENST00000354115.6:c.379T=	ENSP00000329072.3:p.Phe127=
ENST00000361779.7:c.331T=	ENSP00000354816.3:p.Phe111=
ENST00000409052.5:c.331T=	ENSP00000387210.1:p.Phe111=
ENST00000409930.3:c.433T=	ENSP00000387173.3:p.Phe145=
NM_000577.4:c.379T=	NP_000568.1:p.Phe127=
NM_173841.2:c.442T= , LRG_188t1:c.442T=	NP_776213.1:p.Phe148=
NM_173842.2:c.433T=	NP_776214.1:p.Phe145=
NM_173843.2:c.331T=	NP_776215.1:p.Phe111=
XM_005263661.3:c.331T=	XP_005263718.1:p.Phe111=
XM_006712497.2:c.331T=	XP_006712560.1:p.Phe111=
XM_011511121.1:c.331T=	XP_011509423.1:p.Phe111=
NM_001318914.1:c.331T=	NP_001305843.1:p.Phe111=
XM_005263661.4:c.331T=	XP_005263718.1:p.Phe111=
NM_000577.5:c.379T=	NP_000568.1:p.Phe127=
NM_001318914.2:c.331T=	NP_001305843.1:p.Phe111=
NM_173842.3:c.433T= MANE Select	NP_776214.1:p.Phe145=
NM_173843.3:c.331T=	NP_776215.1:p.Phe111=
NM_001379360.1:c.331T=	NP_001366289.1:p.Phe111=
NM_173841.3:c.442T=	NP_776213.1:p.Phe148=