Canonical Allele Identifier: CA755278497

Gene: IL1RN

Linked Data

• dbSNP Id: rs1225124473
• MyVariant Identifiers: chr2:g.113891425_113891426insGCAGA (hg19) ; chr2:g.113133848_113133849insGCAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133853_113133857dup , CM000664.2:g.113133853_113133857dup	GRCh38
NC_000002.11:g.113891430_113891434dup , CM000664.1:g.113891430_113891434dup	GRCh37
NC_000002.10:g.113607901_113607905dup	NCBI36
NG_021240.1:g.20961_20965dup , LRG_188:g.20961_20965dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*840_*844dup	ENSP00000387210.1:n.*840_*844dup
ENST00000696880.1:c.*519_*523dup	ENSP00000512948.1:n.*519_*523dup
ENST00000409930.4:c.*982_*986dup MANE Select	ENSP00000387173.3:n.*982_*986dup
ENST00000259206.9:c.*982_*986dup	ENSP00000259206.5:n.*982_*986dup
ENST00000354115.6:c.*982_*986dup	ENSP00000329072.3:n.*982_*986dup
ENST00000361779.7:c.*982_*986dup	ENSP00000354816.3:n.*982_*986dup
ENST00000409052.5:c.*840_*844dup	ENSP00000387210.1:n.*840_*844dup
NM_000577.4:c.*982_*986dup	NP_000568.1:n.*982_*986dup
NM_173841.2:c.*982_*986dup , LRG_188t1:c.*982_*986dup	NP_776213.1:n.*982_*986dup
NM_173842.2:c.*982_*986dup	NP_776214.1:n.*982_*986dup
NM_173843.2:c.*982_*986dup	NP_776215.1:n.*982_*986dup
XM_005263661.3:c.*982_*986dup	XP_005263718.1:n.*982_*986dup
XM_006712497.2:c.*982_*986dup	XP_006712560.1:n.*982_*986dup
XM_011511121.1:c.*982_*986dup	XP_011509423.1:n.*982_*986dup
NM_001318914.1:c.*982_*986dup	NP_001305843.1:n.*982_*986dup
XM_005263661.4:c.*982_*986dup	XP_005263718.1:n.*982_*986dup
NM_000577.5:c.*982_*986dup	NP_000568.1:n.*982_*986dup
NM_001318914.2:c.*982_*986dup	NP_001305843.1:n.*982_*986dup
NM_173842.3:c.*982_*986dup MANE Select	NP_776214.1:n.*982_*986dup
NM_173843.3:c.*982_*986dup	NP_776215.1:n.*982_*986dup
NM_001379360.1:c.*982_*986dup	NP_001366289.1:n.*982_*986dup
NM_173841.3:c.*982_*986dup	NP_776213.1:n.*982_*986dup