Canonical Allele Identifier: CA2751751129

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133188_113133189insAAAAAAAAAAATCATGAAAT , CM000664.2:g.113133188_113133189insAAAAAAAAAAATCATGAAAT	GRCh38
NC_000002.11:g.113890765_113890766insAAAAAAAAAAATCATGAAAT , CM000664.1:g.113890765_113890766insAAAAAAAAAAATCATGAAAT	GRCh37
NC_000002.10:g.113607236_113607237insAAAAAAAAAAATCATGAAAT	NCBI36
NG_021240.1:g.20296_20297insAAAAAAAAAAATCATGAAAT , LRG_188:g.20296_20297insAAAAAAAAAAATCATGAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*317_*318insAAAAAAAAAAATCATGAAAT	ENSP00000387210.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
ENST00000696879.1:c.*317_*318insAAAAAAAAAAATCATGAAAT	ENSP00000512947.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
ENST00000696880.1:c.*211+106_*211+107insAAAAAAAAAAATCATGAAAT	ENSP00000512948.1:n.*211+106_*211+107insAAAAAAAAAAATCATGAAAT
ENST00000696882.1:c.*621_*622insAAAAAAAAAAATCATGAAAT	ENSP00000512950.1:n.*621_*622insAAAAAAAAAAATCATGAAAT
ENST00000409930.4:c.*317_*318insAAAAAAAAAAATCATGAAAT MANE Select	ENSP00000387173.3:n.*317_*318insAAAAAAAAAAATCATGAAAT
ENST00000259206.9:c.*317_*318insAAAAAAAAAAATCATGAAAT	ENSP00000259206.5:n.*317_*318insAAAAAAAAAAATCATGAAAT
ENST00000354115.6:c.*317_*318insAAAAAAAAAAATCATGAAAT	ENSP00000329072.3:n.*317_*318insAAAAAAAAAAATCATGAAAT
ENST00000361779.7:c.*317_*318insAAAAAAAAAAATCATGAAAT	ENSP00000354816.3:n.*317_*318insAAAAAAAAAAATCATGAAAT
ENST00000409052.5:c.*317_*318insAAAAAAAAAAATCATGAAAT	ENSP00000387210.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_000577.4:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_000568.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_173841.2:c.*317_*318insAAAAAAAAAAATCATGAAAT , LRG_188t1:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_776213.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_173842.2:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_776214.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_173843.2:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_776215.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
XM_005263661.3:c.*317_*318insAAAAAAAAAAATCATGAAAT	XP_005263718.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
XM_006712497.2:c.*317_*318insAAAAAAAAAAATCATGAAAT	XP_006712560.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
XM_011511121.1:c.*317_*318insAAAAAAAAAAATCATGAAAT	XP_011509423.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_001318914.1:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_001305843.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
XM_005263661.4:c.*317_*318insAAAAAAAAAAATCATGAAAT	XP_005263718.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_000577.5:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_000568.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_001318914.2:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_001305843.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_173842.3:c.*317_*318insAAAAAAAAAAATCATGAAAT MANE Select	NP_776214.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_173843.3:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_776215.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_001379360.1:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_001366289.1:n.*317_*318insAAAAAAAAAAATCATGAAAT
NM_173841.3:c.*317_*318insAAAAAAAAAAATCATGAAAT	NP_776213.1:n.*317_*318insAAAAAAAAAAATCATGAAAT