Canonical Allele Identifier: CA2660766571

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113133876-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133879_113133880del , CM000664.2:g.113133879_113133880del	GRCh38
NC_000002.11:g.113891456_113891457del , CM000664.1:g.113891456_113891457del	GRCh37
NC_000002.10:g.113607927_113607928del	NCBI36
NG_021240.1:g.20987_20988del , LRG_188:g.20987_20988del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*866_*867del	ENSP00000387210.1:n.*866_*867del
ENST00000696880.1:c.*545_*546del	ENSP00000512948.1:n.*545_*546del
ENST00000409930.4:c.*1008_*1009del MANE Select	ENSP00000387173.3:n.*1008_*1009del
ENST00000259206.9:c.*1008_*1009del	ENSP00000259206.5:n.*1008_*1009del
ENST00000354115.6:c.*1008_*1009del	ENSP00000329072.3:n.*1008_*1009del
ENST00000361779.7:c.*1008_*1009del	ENSP00000354816.3:n.*1008_*1009del
ENST00000409052.5:c.*866_*867del	ENSP00000387210.1:n.*866_*867del
NM_000577.4:c.*1008_*1009del	NP_000568.1:n.*1008_*1009del
NM_173841.2:c.*1008_*1009del , LRG_188t1:c.*1008_*1009del	NP_776213.1:n.*1008_*1009del
NM_173842.2:c.*1008_*1009del	NP_776214.1:n.*1008_*1009del
NM_173843.2:c.*1008_*1009del	NP_776215.1:n.*1008_*1009del
XM_005263661.3:c.*1008_*1009del	XP_005263718.1:n.*1008_*1009del
XM_006712497.2:c.*1008_*1009del	XP_006712560.1:n.*1008_*1009del
XM_011511121.1:c.*1008_*1009del	XP_011509423.1:n.*1008_*1009del
NM_001318914.1:c.*1008_*1009del	NP_001305843.1:n.*1008_*1009del
XM_005263661.4:c.*1008_*1009del	XP_005263718.1:n.*1008_*1009del
NM_000577.5:c.*1008_*1009del	NP_000568.1:n.*1008_*1009del
NM_001318914.2:c.*1008_*1009del	NP_001305843.1:n.*1008_*1009del
NM_173842.3:c.*1008_*1009del MANE Select	NP_776214.1:n.*1008_*1009del
NM_173843.3:c.*1008_*1009del	NP_776215.1:n.*1008_*1009del
NM_001379360.1:c.*1008_*1009del	NP_001366289.1:n.*1008_*1009del
NM_173841.3:c.*1008_*1009del	NP_776213.1:n.*1008_*1009del