Canonical Allele Identifier: CA348296073
Gene: IL1RN HGNC NCBI

Linked Data

ClinVar Variation Id: 1037248
ClinVar RCV Id: RCV001340372
dbSNP Id: rs1687216601

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113132725A>G , CM000664.2:g.113132725A>G GRCh38
NC_000002.11:g.113890302A>G , CM000664.1:g.113890302A>G GRCh37
NC_000002.10:g.113606773A>G NCBI36
NG_021240.1:g.19833A>G , LRG_188:g.19833A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.286A>G ENSP00000387210.1:p.Ser96Gly
ENST00000696879.1:c.286A>G ENSP00000512947.1:p.Ser96Gly
ENST00000696880.1:c.286A>G ENSP00000512948.1:p.Ser96Gly
ENST00000696881.1:c.286A>G ENSP00000512949.1:p.Ser96Gly
ENST00000696882.1:c.*158A>G ENSP00000512950.1:n.*158A>G
ENST00000696883.1:n.333A>G
ENST00000409930.4:c.388A>G MANE Select ENSP00000387173.3:p.Ser130Gly
ENST00000259206.9:c.397A>G ENSP00000259206.5:p.Ser133Gly
ENST00000354115.6:c.334A>G ENSP00000329072.3:p.Ser112Gly
ENST00000361779.7:c.286A>G ENSP00000354816.3:p.Ser96Gly
ENST00000409052.5:c.286A>G ENSP00000387210.1:p.Ser96Gly
ENST00000409930.3:c.388A>G ENSP00000387173.3:p.Ser130Gly
NM_000577.4:c.334A>G NP_000568.1:p.Ser112Gly
NM_173841.2:c.397A>G , LRG_188t1:c.397A>G NP_776213.1:p.Ser133Gly
NM_173842.2:c.388A>G NP_776214.1:p.Ser130Gly
NM_173843.2:c.286A>G NP_776215.1:p.Ser96Gly
XM_005263661.3:c.286A>G XP_005263718.1:p.Ser96Gly
XM_006712497.2:c.286A>G XP_006712560.1:p.Ser96Gly
XM_011511121.1:c.286A>G XP_011509423.1:p.Ser96Gly
NM_001318914.1:c.286A>G NP_001305843.1:p.Ser96Gly
XM_005263661.4:c.286A>G XP_005263718.1:p.Ser96Gly
NM_000577.5:c.334A>G NP_000568.1:p.Ser112Gly
NM_001318914.2:c.286A>G NP_001305843.1:p.Ser96Gly
NM_173842.3:c.388A>G MANE Select NP_776214.1:p.Ser130Gly
NM_173843.3:c.286A>G NP_776215.1:p.Ser96Gly
NM_001379360.1:c.286A>G NP_001366289.1:p.Ser96Gly
NM_173841.3:c.397A>G NP_776213.1:p.Ser133Gly