Canonical Allele Identifier: CA2660765821

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113132729-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132733del , CM000664.2:g.113132733del	GRCh38
NC_000002.11:g.113890310del , CM000664.1:g.113890310del	GRCh37
NC_000002.10:g.113606781del	NCBI36
NG_021240.1:g.19841del , LRG_188:g.19841del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.294del	ENSP00000387210.1:p.Thr99ProfsTer?
ENST00000696879.1:c.294del	ENSP00000512947.1:p.Thr99ProfsTer?
ENST00000696880.1:c.294del	ENSP00000512948.1:p.Thr99ProfsTer?
ENST00000696881.1:c.294del	ENSP00000512949.1:p.Thr99ProfsTer?
ENST00000696882.1:c.*166del	ENSP00000512950.1:n.*166del
ENST00000696883.1:n.341del
ENST00000409930.4:c.396del MANE Select	ENSP00000387173.3:p.Thr133ProfsTer?
ENST00000259206.9:c.405del	ENSP00000259206.5:p.Thr136ProfsTer?
ENST00000354115.6:c.342del	ENSP00000329072.3:p.Thr115ProfsTer?
ENST00000361779.7:c.294del	ENSP00000354816.3:p.Thr99ProfsTer?
ENST00000409052.5:c.294del	ENSP00000387210.1:p.Thr99ProfsTer?
ENST00000409930.3:c.396del	ENSP00000387173.3:p.Thr133ProfsTer?
NM_000577.4:c.342del	NP_000568.1:p.Thr115ProfsTer?
NM_173841.2:c.405del , LRG_188t1:c.405del	NP_776213.1:p.Thr136ProfsTer?
NM_173842.2:c.396del	NP_776214.1:p.Thr133ProfsTer?
NM_173843.2:c.294del	NP_776215.1:p.Thr99ProfsTer?
XM_005263661.3:c.294del	XP_005263718.1:p.Thr99ProfsTer?
XM_006712497.2:c.294del	XP_006712560.1:p.Thr99ProfsTer?
XM_011511121.1:c.294del	XP_011509423.1:p.Thr99ProfsTer?
NM_001318914.1:c.294del	NP_001305843.1:p.Thr99ProfsTer?
XM_005263661.4:c.294del	XP_005263718.1:p.Thr99ProfsTer?
NM_000577.5:c.342del	NP_000568.1:p.Thr115ProfsTer?
NM_001318914.2:c.294del	NP_001305843.1:p.Thr99ProfsTer?
NM_173842.3:c.396del MANE Select	NP_776214.1:p.Thr133ProfsTer?
NM_173843.3:c.294del	NP_776215.1:p.Thr99ProfsTer?
NM_001379360.1:c.294del	NP_001366289.1:p.Thr99ProfsTer?
NM_173841.3:c.405del	NP_776213.1:p.Thr136ProfsTer?