Canonical Allele Identifier: CA2660766400

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113133614-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133614C>A , CM000664.2:g.113133614C>A	GRCh38
NC_000002.11:g.113891191C>A , CM000664.1:g.113891191C>A	GRCh37
NC_000002.10:g.113607662C>A	NCBI36
NG_021240.1:g.20722C>A , LRG_188:g.20722C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*601C>A	ENSP00000387210.1:n.*601C>A
ENST00000696880.1:c.*308-28C>A	ENSP00000512948.1:n.*308-28C>A
ENST00000409930.4:c.*743C>A MANE Select	ENSP00000387173.3:n.*743C>A
ENST00000259206.9:c.*743C>A	ENSP00000259206.5:n.*743C>A
ENST00000354115.6:c.*743C>A	ENSP00000329072.3:n.*743C>A
ENST00000361779.7:c.*743C>A	ENSP00000354816.3:n.*743C>A
ENST00000409052.5:c.*601C>A	ENSP00000387210.1:n.*601C>A
NM_000577.4:c.*743C>A	NP_000568.1:n.*743C>A
NM_173841.2:c.*743C>A , LRG_188t1:c.*743C>A	NP_776213.1:n.*743C>A
NM_173842.2:c.*743C>A	NP_776214.1:n.*743C>A
NM_173843.2:c.*743C>A	NP_776215.1:n.*743C>A
XM_005263661.3:c.*743C>A	XP_005263718.1:n.*743C>A
XM_006712497.2:c.*743C>A	XP_006712560.1:n.*743C>A
XM_011511121.1:c.*743C>A	XP_011509423.1:n.*743C>A
NM_001318914.1:c.*743C>A	NP_001305843.1:n.*743C>A
XM_005263661.4:c.*743C>A	XP_005263718.1:n.*743C>A
NM_000577.5:c.*743C>A	NP_000568.1:n.*743C>A
NM_001318914.2:c.*743C>A	NP_001305843.1:n.*743C>A
NM_173842.3:c.*743C>A MANE Select	NP_776214.1:n.*743C>A
NM_173843.3:c.*743C>A	NP_776215.1:n.*743C>A
NM_001379360.1:c.*743C>A	NP_001366289.1:n.*743C>A
NM_173841.3:c.*743C>A	NP_776213.1:n.*743C>A