Canonical Allele Identifier: CA1280070556
Gene: IL1RN HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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