Canonical Allele Identifier: CA53697220

Gene: IL1RN

Linked Data

• dbSNP Id: rs774086690
• gnomAD v2: 2-113889925-T-TGAGGCAGGAGAATCGCTTG
• gnomAD v3: 2-113132348-T-TGAGGCAGGAGAATCGCTTG
• gnomAD v4: 2-113132348-T-TGAGGCAGGAGAATCGCTTG
• MyVariant Identifiers: chr2:g.113889925_113889926insGAGGCAGGAGAATCGCTTG (hg19) ; chr2:g.113132348_113132349insGAGGCAGGAGAATCGCTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132349_113132367dup , CM000664.2:g.113132349_113132367dup	GRCh38
NC_000002.11:g.113889926_113889944dup , CM000664.1:g.113889926_113889944dup	GRCh37
NC_000002.10:g.113606397_113606415dup	NCBI36
NG_021240.1:g.19457_19475dup , LRG_188:g.19457_19475dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.217-307_217-289dup	ENSP00000387210.1:n.217-307_217-289dup
ENST00000696879.1:c.217-307_217-289dup	ENSP00000512947.1:n.217-307_217-289dup
ENST00000696880.1:c.217-307_217-289dup	ENSP00000512948.1:n.217-307_217-289dup
ENST00000696881.1:c.217-307_217-289dup	ENSP00000512949.1:n.217-307_217-289dup
ENST00000696882.1:c.*89-307_*89-289dup	ENSP00000512950.1:n.*89-307_*89-289dup
ENST00000696883.1:n.264-307_264-289dup
ENST00000409930.4:c.319-307_319-289dup MANE Select	ENSP00000387173.3:n.319-307_319-289dup
ENST00000259206.9:c.328-307_328-289dup	ENSP00000259206.5:n.328-307_328-289dup
ENST00000354115.6:c.265-307_265-289dup	ENSP00000329072.3:n.265-307_265-289dup
ENST00000361779.7:c.217-307_217-289dup	ENSP00000354816.3:n.217-307_217-289dup
ENST00000409052.5:c.217-307_217-289dup	ENSP00000387210.1:n.217-307_217-289dup
ENST00000409930.3:c.319-307_319-289dup	ENSP00000387173.3:n.319-307_319-289dup
NM_000577.4:c.265-307_265-289dup	NP_000568.1:n.265-307_265-289dup
NM_173841.2:c.328-307_328-289dup , LRG_188t1:c.328-307_328-289dup	NP_776213.1:n.328-307_328-289dup
NM_173842.2:c.319-307_319-289dup	NP_776214.1:n.319-307_319-289dup
NM_173843.2:c.217-307_217-289dup	NP_776215.1:n.217-307_217-289dup
XM_005263661.3:c.217-307_217-289dup	XP_005263718.1:n.217-307_217-289dup
XM_006712497.2:c.217-307_217-289dup	XP_006712560.1:n.217-307_217-289dup
XM_011511121.1:c.217-307_217-289dup	XP_011509423.1:n.217-307_217-289dup
NM_001318914.1:c.217-307_217-289dup	NP_001305843.1:n.217-307_217-289dup
XM_005263661.4:c.217-307_217-289dup	XP_005263718.1:n.217-307_217-289dup
NM_000577.5:c.265-307_265-289dup	NP_000568.1:n.265-307_265-289dup
NM_001318914.2:c.217-307_217-289dup	NP_001305843.1:n.217-307_217-289dup
NM_173842.3:c.319-307_319-289dup MANE Select	NP_776214.1:n.319-307_319-289dup
NM_173843.3:c.217-307_217-289dup	NP_776215.1:n.217-307_217-289dup
NM_001379360.1:c.217-307_217-289dup	NP_001366289.1:n.217-307_217-289dup
NM_173841.3:c.328-307_328-289dup	NP_776213.1:n.328-307_328-289dup