Canonical Allele Identifier: CA1280068145
Gene: IL1RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113121602C= , CM000664.2:g.113121602C= GRCh38
NC_000002.11:g.113879179C= , CM000664.1:g.113879179C= GRCh37
NC_000002.10:g.113595650C= NCBI36
NG_021240.1:g.8710C= , LRG_188:g.8710C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.-55C= ENSP00000387210.1:n.-55C=
ENST00000696881.1:c.-55C= ENSP00000512949.1:n.-55C=
ENST00000259206.9:c.73+1474C= ENSP00000259206.5:n.73+1474C=
ENST00000354115.6:c.10+3574C= ENSP00000329072.3:n.10+3574C=
ENST00000361779.7:c.-55C= ENSP00000354816.3:n.-55C=
ENST00000409052.5:c.-55C= ENSP00000387210.1:n.-55C=
ENST00000486167.1:n.48+3574C=
NM_000577.4:c.10+3574C= NP_000568.1:n.10+3574C=
NM_173841.2:c.73+1474C= , LRG_188t1:c.73+1474C= NP_776213.1:n.73+1474C=
NM_173843.2:c.-55C= NP_776215.1:n.-55C=
XM_006712497.2:c.-55C= XP_006712560.1:n.-55C=
XM_011511121.1:c.-55C= XP_011509423.1:n.-55C=
NM_001318914.1:c.-55C= NP_001305843.1:n.-55C=
NM_000577.5:c.10+3574C= NP_000568.1:n.10+3574C=
NM_001318914.2:c.-55C= NP_001305843.1:n.-55C=
NM_173843.3:c.-55C= NP_776215.1:n.-55C=
NM_173841.3:c.73+1474C= NP_776213.1:n.73+1474C=