Canonical Allele Identifier: CA2660764742

Gene: IL1RN

Linked Data

• ClinVar Variation Id: 3018138
• ClinVar RCV Id: RCV003876801
• gnomAD v4: 2-113127750-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113127750C>A , CM000664.2:g.113127750C>A	GRCh38
NC_000002.11:g.113885327C>A , CM000664.1:g.113885327C>A	GRCh37
NC_000002.10:g.113601798C>A	NCBI36
NG_021240.1:g.14858C>A , LRG_188:g.14858C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.14+10C>A	ENSP00000387210.1:n.14+10C>A
ENST00000696879.1:c.14+10C>A	ENSP00000512947.1:n.14+10C>A
ENST00000696880.1:c.14+10C>A	ENSP00000512948.1:n.14+10C>A
ENST00000696881.1:c.14+10C>A	ENSP00000512949.1:n.14+10C>A
ENST00000696882.1:c.14+10C>A	ENSP00000512950.1:n.14+10C>A
ENST00000409930.4:c.116+10C>A MANE Select	ENSP00000387173.3:n.116+10C>A
ENST00000259206.9:c.125+10C>A	ENSP00000259206.5:n.125+10C>A
ENST00000354115.6:c.62+10C>A	ENSP00000329072.3:n.62+10C>A
ENST00000361779.7:c.14+10C>A	ENSP00000354816.3:n.14+10C>A
ENST00000409052.5:c.14+10C>A	ENSP00000387210.1:n.14+10C>A
ENST00000409930.3:c.116+10C>A	ENSP00000387173.3:n.116+10C>A
ENST00000472292.1:n.165+10C>A
ENST00000486167.1:n.100+10C>A
NM_000577.4:c.62+10C>A	NP_000568.1:n.62+10C>A
NM_173841.2:c.125+10C>A , LRG_188t1:c.125+10C>A	NP_776213.1:n.125+10C>A
NM_173842.2:c.116+10C>A	NP_776214.1:n.116+10C>A
NM_173843.2:c.14+10C>A	NP_776215.1:n.14+10C>A
XM_005263661.3:c.14+10C>A	XP_005263718.1:n.14+10C>A
XM_006712497.2:c.14+10C>A	XP_006712560.1:n.14+10C>A
XM_011511121.1:c.14+10C>A	XP_011509423.1:n.14+10C>A
NM_001318914.1:c.14+10C>A	NP_001305843.1:n.14+10C>A
XM_005263661.4:c.14+10C>A	XP_005263718.1:n.14+10C>A
NM_000577.5:c.62+10C>A	NP_000568.1:n.62+10C>A
NM_001318914.2:c.14+10C>A	NP_001305843.1:n.14+10C>A
NM_173842.3:c.116+10C>A MANE Select	NP_776214.1:n.116+10C>A
NM_173843.3:c.14+10C>A	NP_776215.1:n.14+10C>A
NM_001379360.1:c.14+10C>A	NP_001366289.1:n.14+10C>A
NM_173841.3:c.125+10C>A	NP_776213.1:n.125+10C>A