Canonical Allele Identifier: CA1280070554
Gene: IL1RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113126824G= , CM000664.2:g.113126824G= GRCh38
NC_000002.11:g.113884401G= , CM000664.1:g.113884401G= GRCh37
NC_000002.10:g.113600872G= NCBI36
NG_021240.1:g.13932G= , LRG_188:g.13932G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-38-865G= ENSP00000387210.1:n.-38-865G=
ENST00000696881.1:c.-38-865G= ENSP00000512949.1:n.-38-865G=
ENST00000259206.9:c.74-865G= ENSP00000259206.5:n.74-865G=
ENST00000354115.6:c.11-865G= ENSP00000329072.3:n.11-865G=
ENST00000361779.7:c.-38-865G= ENSP00000354816.3:n.-38-865G=
ENST00000409052.5:c.-38-865G= ENSP00000387210.1:n.-38-865G=
ENST00000486167.1:n.49-865G=
NM_000577.4:c.11-865G= NP_000568.1:n.11-865G=
NM_173841.2:c.74-865G= , LRG_188t1:c.74-865G= NP_776213.1:n.74-865G=
NM_173843.2:c.-38-865G= NP_776215.1:n.-38-865G=
XM_005263661.3:c.-765G= XP_005263718.1:n.-765G=
XM_006712497.2:c.-38-865G= XP_006712560.1:n.-38-865G=
XM_011511121.1:c.-38-865G= XP_011509423.1:n.-38-865G=
NM_001318914.1:c.-38-865G= NP_001305843.1:n.-38-865G=
NM_000577.5:c.11-865G= NP_000568.1:n.11-865G=
NM_001318914.2:c.-38-865G= NP_001305843.1:n.-38-865G=
NM_173843.3:c.-38-865G= NP_776215.1:n.-38-865G=
NM_173841.3:c.74-865G= NP_776213.1:n.74-865G=