Canonical Allele Identifier: CA1280072485
Gene: IL1RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113130974A= , CM000664.2:g.113130974A= GRCh38
NC_000002.11:g.113888551A= , CM000664.1:g.113888551A= GRCh37
NC_000002.10:g.113605022A= NCBI36
NG_021240.1:g.18082A= , LRG_188:g.18082A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409052.6:c.104-71A= ENSP00000387210.1:n.104-71A=
ENST00000696879.1:c.104-71A= ENSP00000512947.1:n.104-71A=
ENST00000696880.1:c.104-71A= ENSP00000512948.1:n.104-71A=
ENST00000696881.1:c.104-71A= ENSP00000512949.1:n.104-71A=
ENST00000696882.1:c.104-76A= ENSP00000512950.1:n.104-76A=
ENST00000696883.1:n.80A=
ENST00000409930.4:c.206-71A= MANE Select ENSP00000387173.3:n.206-71A=
ENST00000259206.9:c.215-71A= ENSP00000259206.5:n.215-71A=
ENST00000354115.6:c.152-71A= ENSP00000329072.3:n.152-71A=
ENST00000361779.7:c.104-71A= ENSP00000354816.3:n.104-71A=
ENST00000409052.5:c.104-71A= ENSP00000387210.1:n.104-71A=
ENST00000409930.3:c.206-71A= ENSP00000387173.3:n.206-71A=
NM_000577.4:c.152-71A= NP_000568.1:n.152-71A=
NM_173841.2:c.215-71A= , LRG_188t1:c.215-71A= NP_776213.1:n.215-71A=
NM_173842.2:c.206-71A= NP_776214.1:n.206-71A=
NM_173843.2:c.104-71A= NP_776215.1:n.104-71A=
XM_005263661.3:c.104-71A= XP_005263718.1:n.104-71A=
XM_006712497.2:c.104-71A= XP_006712560.1:n.104-71A=
XM_011511121.1:c.104-71A= XP_011509423.1:n.104-71A=
NM_001318914.1:c.104-71A= NP_001305843.1:n.104-71A=
XM_005263661.4:c.104-71A= XP_005263718.1:n.104-71A=
NM_000577.5:c.152-71A= NP_000568.1:n.152-71A=
NM_001318914.2:c.104-71A= NP_001305843.1:n.104-71A=
NM_173842.3:c.206-71A= MANE Select NP_776214.1:n.206-71A=
NM_173843.3:c.104-71A= NP_776215.1:n.104-71A=
NM_001379360.1:c.104-71A= NP_001366289.1:n.104-71A=
NM_173841.3:c.215-71A= NP_776213.1:n.215-71A=