Canonical Allele Identifier: CA348296052
Gene: IL1RN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113132719T>C , CM000664.2:g.113132719T>C GRCh38
NC_000002.11:g.113890296T>C , CM000664.1:g.113890296T>C GRCh37
NC_000002.10:g.113606767T>C NCBI36
NG_021240.1:g.19827T>C , LRG_188:g.19827T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.280T>C ENSP00000387210.1:p.Ser94Pro
ENST00000696879.1:c.280T>C ENSP00000512947.1:p.Ser94Pro
ENST00000696880.1:c.280T>C ENSP00000512948.1:p.Ser94Pro
ENST00000696881.1:c.280T>C ENSP00000512949.1:p.Ser94Pro
ENST00000696882.1:c.*152T>C ENSP00000512950.1:n.*152T>C
ENST00000696883.1:n.327T>C
ENST00000409930.4:c.382T>C MANE Select ENSP00000387173.3:p.Ser128Pro
ENST00000259206.9:c.391T>C ENSP00000259206.5:p.Ser131Pro
ENST00000354115.6:c.328T>C ENSP00000329072.3:p.Ser110Pro
ENST00000361779.7:c.280T>C ENSP00000354816.3:p.Ser94Pro
ENST00000409052.5:c.280T>C ENSP00000387210.1:p.Ser94Pro
ENST00000409930.3:c.382T>C ENSP00000387173.3:p.Ser128Pro
NM_000577.4:c.328T>C NP_000568.1:p.Ser110Pro
NM_173841.2:c.391T>C , LRG_188t1:c.391T>C NP_776213.1:p.Ser131Pro
NM_173842.2:c.382T>C NP_776214.1:p.Ser128Pro
NM_173843.2:c.280T>C NP_776215.1:p.Ser94Pro
XM_005263661.3:c.280T>C XP_005263718.1:p.Ser94Pro
XM_006712497.2:c.280T>C XP_006712560.1:p.Ser94Pro
XM_011511121.1:c.280T>C XP_011509423.1:p.Ser94Pro
NM_001318914.1:c.280T>C NP_001305843.1:p.Ser94Pro
XM_005263661.4:c.280T>C XP_005263718.1:p.Ser94Pro
NM_000577.5:c.328T>C NP_000568.1:p.Ser110Pro
NM_001318914.2:c.280T>C NP_001305843.1:p.Ser94Pro
NM_173842.3:c.382T>C MANE Select NP_776214.1:p.Ser128Pro
NM_173843.3:c.280T>C NP_776215.1:p.Ser94Pro
NM_001379360.1:c.280T>C NP_001366289.1:p.Ser94Pro
NM_173841.3:c.391T>C NP_776213.1:p.Ser131Pro