Canonical Allele Identifier: CA2700213190

Gene: IL1RN

Linked Data

• dbSNP Id: rs2104462807

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132839del , CM000664.2:g.113132839del	GRCh38
NC_000002.11:g.113890416del , CM000664.1:g.113890416del	GRCh37
NC_000002.10:g.113606887del	NCBI36
NG_021240.1:g.19947del , LRG_188:g.19947del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.400del	ENSP00000387210.1:p.Val134SerfsTer?
ENST00000696879.1:c.400del	ENSP00000512947.1:p.Val134SerfsTer?
ENST00000696880.1:c.400del	ENSP00000512948.1:p.Val134SerfsTer?
ENST00000696881.1:c.400del	ENSP00000512949.1:p.Val134SerfsTer?
ENST00000696882.1:c.*272del	ENSP00000512950.1:n.*272del
ENST00000696883.1:n.447del
ENST00000409930.4:c.502del MANE Select	ENSP00000387173.3:p.Val168SerfsTer?
ENST00000259206.9:c.511del	ENSP00000259206.5:p.Val171SerfsTer?
ENST00000354115.6:c.448del	ENSP00000329072.3:p.Val150SerfsTer?
ENST00000361779.7:c.400del	ENSP00000354816.3:p.Val134SerfsTer?
ENST00000409052.5:c.400del	ENSP00000387210.1:p.Val134SerfsTer?
ENST00000409930.3:c.502del	ENSP00000387173.3:p.Val168SerfsTer?
NM_000577.4:c.448del	NP_000568.1:p.Val150SerfsTer?
NM_173841.2:c.511del , LRG_188t1:c.511del	NP_776213.1:p.Val171SerfsTer?
NM_173842.2:c.502del	NP_776214.1:p.Val168SerfsTer?
NM_173843.2:c.400del	NP_776215.1:p.Val134SerfsTer?
XM_005263661.3:c.400del	XP_005263718.1:p.Val134SerfsTer?
XM_006712497.2:c.400del	XP_006712560.1:p.Val134SerfsTer?
XM_011511121.1:c.400del	XP_011509423.1:p.Val134SerfsTer?
NM_001318914.1:c.400del	NP_001305843.1:p.Val134SerfsTer?
XM_005263661.4:c.400del	XP_005263718.1:p.Val134SerfsTer?
NM_000577.5:c.448del	NP_000568.1:p.Val150SerfsTer?
NM_001318914.2:c.400del	NP_001305843.1:p.Val134SerfsTer?
NM_173842.3:c.502del MANE Select	NP_776214.1:p.Val168SerfsTer?
NM_173843.3:c.400del	NP_776215.1:p.Val134SerfsTer?
NM_001379360.1:c.400del	NP_001366289.1:p.Val134SerfsTer?
NM_173841.3:c.511del	NP_776213.1:p.Val171SerfsTer?