Canonical Allele Identifier: CA755277966

Gene: IL1RN

Linked Data

• dbSNP Id: rs1340075049
• gnomAD v3: 2-113132876-GC-G
• gnomAD v4: 2-113132876-GC-G
• MyVariant Identifiers: chr2:g.113890454del (hg19) ; chr2:g.113132877del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132879del , CM000664.2:g.113132879del	GRCh38
NC_000002.11:g.113890456del , CM000664.1:g.113890456del	GRCh37
NC_000002.10:g.113606927del	NCBI36
NG_021240.1:g.19987del , LRG_188:g.19987del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*8del	ENSP00000387210.1:n.*8del
ENST00000696879.1:c.*8del	ENSP00000512947.1:n.*8del
ENST00000696880.1:c.*8del	ENSP00000512948.1:n.*8del
ENST00000696881.1:c.*8del	ENSP00000512949.1:n.*8del
ENST00000696882.1:c.*312del	ENSP00000512950.1:n.*312del
ENST00000696883.1:n.487del
ENST00000409930.4:c.*8del MANE Select	ENSP00000387173.3:n.*8del
ENST00000259206.9:c.*8del	ENSP00000259206.5:n.*8del
ENST00000354115.6:c.*8del	ENSP00000329072.3:n.*8del
ENST00000361779.7:c.*8del	ENSP00000354816.3:n.*8del
ENST00000409052.5:c.*8del	ENSP00000387210.1:n.*8del
ENST00000409930.3:c.*8del	ENSP00000387173.3:n.*8del
NM_000577.4:c.*8del	NP_000568.1:n.*8del
NM_173841.2:c.*8del , LRG_188t1:c.*8del	NP_776213.1:n.*8del
NM_173842.2:c.*8del	NP_776214.1:n.*8del
NM_173843.2:c.*8del	NP_776215.1:n.*8del
XM_005263661.3:c.*8del	XP_005263718.1:n.*8del
XM_006712497.2:c.*8del	XP_006712560.1:n.*8del
XM_011511121.1:c.*8del	XP_011509423.1:n.*8del
NM_001318914.1:c.*8del	NP_001305843.1:n.*8del
XM_005263661.4:c.*8del	XP_005263718.1:n.*8del
NM_000577.5:c.*8del	NP_000568.1:n.*8del
NM_001318914.2:c.*8del	NP_001305843.1:n.*8del
NM_173842.3:c.*8del MANE Select	NP_776214.1:n.*8del
NM_173843.3:c.*8del	NP_776215.1:n.*8del
NM_001379360.1:c.*8del	NP_001366289.1:n.*8del
NM_173841.3:c.*8del	NP_776213.1:n.*8del