Canonical Allele Identifier: CA348296345

Gene: IL1RN

Linked Data

• MyVariant Identifiers: chr2:g.113890425T>G (hg19) ; chr2:g.113132848T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132848T>G , CM000664.2:g.113132848T>G	GRCh38
NC_000002.11:g.113890425T>G , CM000664.1:g.113890425T>G	GRCh37
NC_000002.10:g.113606896T>G	NCBI36
NG_021240.1:g.19956T>G , LRG_188:g.19956T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.409T>G	ENSP00000387210.1:p.Phe137Val
ENST00000696879.1:c.409T>G	ENSP00000512947.1:p.Phe137Val
ENST00000696880.1:c.409T>G	ENSP00000512948.1:p.Phe137Val
ENST00000696881.1:c.409T>G	ENSP00000512949.1:p.Phe137Val
ENST00000696882.1:c.*281T>G	ENSP00000512950.1:n.*281T>G
ENST00000696883.1:n.456T>G
ENST00000409930.4:c.511T>G MANE Select	ENSP00000387173.3:p.Phe171Val
ENST00000259206.9:c.520T>G	ENSP00000259206.5:p.Phe174Val
ENST00000354115.6:c.457T>G	ENSP00000329072.3:p.Phe153Val
ENST00000361779.7:c.409T>G	ENSP00000354816.3:p.Phe137Val
ENST00000409052.5:c.409T>G	ENSP00000387210.1:p.Phe137Val
ENST00000409930.3:c.511T>G	ENSP00000387173.3:p.Phe171Val
NM_000577.4:c.457T>G	NP_000568.1:p.Phe153Val
NM_173841.2:c.520T>G , LRG_188t1:c.520T>G	NP_776213.1:p.Phe174Val
NM_173842.2:c.511T>G	NP_776214.1:p.Phe171Val
NM_173843.2:c.409T>G	NP_776215.1:p.Phe137Val
XM_005263661.3:c.409T>G	XP_005263718.1:p.Phe137Val
XM_006712497.2:c.409T>G	XP_006712560.1:p.Phe137Val
XM_011511121.1:c.409T>G	XP_011509423.1:p.Phe137Val
NM_001318914.1:c.409T>G	NP_001305843.1:p.Phe137Val
XM_005263661.4:c.409T>G	XP_005263718.1:p.Phe137Val
NM_000577.5:c.457T>G	NP_000568.1:p.Phe153Val
NM_001318914.2:c.409T>G	NP_001305843.1:p.Phe137Val
NM_173842.3:c.511T>G MANE Select	NP_776214.1:p.Phe171Val
NM_173843.3:c.409T>G	NP_776215.1:p.Phe137Val
NM_001379360.1:c.409T>G	NP_001366289.1:p.Phe137Val
NM_173841.3:c.520T>G	NP_776213.1:p.Phe174Val