Canonical Allele Identifier: CA1280073866
Gene: IL1RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113133870G= , CM000664.2:g.113133870G= GRCh38
NC_000002.11:g.113891447G= , CM000664.1:g.113891447G= GRCh37
NC_000002.10:g.113607918G= NCBI36
NG_021240.1:g.20978G= , LRG_188:g.20978G=

Transcript Alleles

HGVS Amino-acid change
ENST00000409052.6:c.*857G= ENSP00000387210.1:n.*857G=
ENST00000696880.1:c.*536G= ENSP00000512948.1:n.*536G=
ENST00000409930.4:c.*999G= MANE Select ENSP00000387173.3:n.*999G=
ENST00000259206.9:c.*999G= ENSP00000259206.5:n.*999G=
ENST00000354115.6:c.*999G= ENSP00000329072.3:n.*999G=
ENST00000361779.7:c.*999G= ENSP00000354816.3:n.*999G=
ENST00000409052.5:c.*857G= ENSP00000387210.1:n.*857G=
NM_000577.4:c.*999G= NP_000568.1:n.*999G=
NM_173841.2:c.*999G= , LRG_188t1:c.*999G= NP_776213.1:n.*999G=
NM_173842.2:c.*999G= NP_776214.1:n.*999G=
NM_173843.2:c.*999G= NP_776215.1:n.*999G=
XM_005263661.3:c.*999G= XP_005263718.1:n.*999G=
XM_006712497.2:c.*999G= XP_006712560.1:n.*999G=
XM_011511121.1:c.*999G= XP_011509423.1:n.*999G=
NM_001318914.1:c.*999G= NP_001305843.1:n.*999G=
XM_005263661.4:c.*999G= XP_005263718.1:n.*999G=
NM_000577.5:c.*999G= NP_000568.1:n.*999G=
NM_001318914.2:c.*999G= NP_001305843.1:n.*999G=
NM_173842.3:c.*999G= MANE Select NP_776214.1:n.*999G=
NM_173843.3:c.*999G= NP_776215.1:n.*999G=
NM_001379360.1:c.*999G= NP_001366289.1:n.*999G=
NM_173841.3:c.*999G= NP_776213.1:n.*999G=