Canonical Allele Identifier: CA2660766453
Gene: IL1RN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113133704_113133708del , CM000664.2:g.113133704_113133708del GRCh38
NC_000002.11:g.113891281_113891285del , CM000664.1:g.113891281_113891285del GRCh37
NC_000002.10:g.113607752_113607756del NCBI36
NG_021240.1:g.20812_20816del , LRG_188:g.20812_20816del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.*691_*695del ENSP00000387210.1:n.*691_*695del
ENST00000696880.1:c.*370_*374del ENSP00000512948.1:n.*370_*374del
ENST00000409930.4:c.*833_*837del MANE Select ENSP00000387173.3:n.*833_*837del
ENST00000259206.9:c.*833_*837del ENSP00000259206.5:n.*833_*837del
ENST00000354115.6:c.*833_*837del ENSP00000329072.3:n.*833_*837del
ENST00000361779.7:c.*833_*837del ENSP00000354816.3:n.*833_*837del
ENST00000409052.5:c.*691_*695del ENSP00000387210.1:n.*691_*695del
NM_000577.4:c.*833_*837del NP_000568.1:n.*833_*837del
NM_173841.2:c.*833_*837del , LRG_188t1:c.*833_*837del NP_776213.1:n.*833_*837del
NM_173842.2:c.*833_*837del NP_776214.1:n.*833_*837del
NM_173843.2:c.*833_*837del NP_776215.1:n.*833_*837del
XM_005263661.3:c.*833_*837del XP_005263718.1:n.*833_*837del
XM_006712497.2:c.*833_*837del XP_006712560.1:n.*833_*837del
XM_011511121.1:c.*833_*837del XP_011509423.1:n.*833_*837del
NM_001318914.1:c.*833_*837del NP_001305843.1:n.*833_*837del
XM_005263661.4:c.*833_*837del XP_005263718.1:n.*833_*837del
NM_000577.5:c.*833_*837del NP_000568.1:n.*833_*837del
NM_001318914.2:c.*833_*837del NP_001305843.1:n.*833_*837del
NM_173842.3:c.*833_*837del MANE Select NP_776214.1:n.*833_*837del
NM_173843.3:c.*833_*837del NP_776215.1:n.*833_*837del
NM_001379360.1:c.*833_*837del NP_001366289.1:n.*833_*837del
NM_173841.3:c.*833_*837del NP_776213.1:n.*833_*837del