Canonical Allele Identifier: CA1035127572
Gene: IL1RN HGNC NCBI

Linked Data

dbSNP Id: rs1687256479

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113133795del , CM000664.2:g.113133795del GRCh38
NC_000002.11:g.113891372del , CM000664.1:g.113891372del GRCh37
NC_000002.10:g.113607843del NCBI36
NG_021240.1:g.20903del , LRG_188:g.20903del

Transcript Alleles

HGVS Amino-acid change
ENST00000409052.6:c.*782del ENSP00000387210.1:n.*782del
ENST00000696880.1:c.*461del ENSP00000512948.1:n.*461del
ENST00000409930.4:c.*924del MANE Select ENSP00000387173.3:n.*924del
ENST00000259206.9:c.*924del ENSP00000259206.5:n.*924del
ENST00000354115.6:c.*924del ENSP00000329072.3:n.*924del
ENST00000361779.7:c.*924del ENSP00000354816.3:n.*924del
ENST00000409052.5:c.*782del ENSP00000387210.1:n.*782del
NM_000577.4:c.*924del NP_000568.1:n.*924del
NM_173841.2:c.*924del , LRG_188t1:c.*924del NP_776213.1:n.*924del
NM_173842.2:c.*924del NP_776214.1:n.*924del
NM_173843.2:c.*924del NP_776215.1:n.*924del
XM_005263661.3:c.*924del XP_005263718.1:n.*924del
XM_006712497.2:c.*924del XP_006712560.1:n.*924del
XM_011511121.1:c.*924del XP_011509423.1:n.*924del
NM_001318914.1:c.*924del NP_001305843.1:n.*924del
XM_005263661.4:c.*924del XP_005263718.1:n.*924del
NM_000577.5:c.*924del NP_000568.1:n.*924del
NM_001318914.2:c.*924del NP_001305843.1:n.*924del
NM_173842.3:c.*924del MANE Select NP_776214.1:n.*924del
NM_173843.3:c.*924del NP_776215.1:n.*924del
NM_001379360.1:c.*924del NP_001366289.1:n.*924del
NM_173841.3:c.*924del NP_776213.1:n.*924del