Canonical Allele Identifier: CA11025321
Gene: IL1RN HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113128773A>G , CM000664.2:g.113128773A>G GRCh38
NC_000002.11:g.113886350A>G , CM000664.1:g.113886350A>G GRCh37
NC_000002.10:g.113602821A>G NCBI36
NG_021240.1:g.15881A>G , LRG_188:g.15881A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409052.6:c.15-803A>G ENSP00000387210.1:n.15-803A>G
ENST00000696879.1:c.15-803A>G ENSP00000512947.1:n.15-803A>G
ENST00000696880.1:c.15-803A>G ENSP00000512948.1:n.15-803A>G
ENST00000696881.1:c.15-803A>G ENSP00000512949.1:n.15-803A>G
ENST00000696882.1:c.15-803A>G ENSP00000512950.1:n.15-803A>G
ENST00000409930.4:c.117-803A>G MANE Select ENSP00000387173.3:n.117-803A>G
ENST00000259206.9:c.126-803A>G ENSP00000259206.5:n.126-803A>G
ENST00000354115.6:c.63-803A>G ENSP00000329072.3:n.63-803A>G
ENST00000361779.7:c.15-803A>G ENSP00000354816.3:n.15-803A>G
ENST00000409052.5:c.15-803A>G ENSP00000387210.1:n.15-803A>G
ENST00000409930.3:c.117-803A>G ENSP00000387173.3:n.117-803A>G
ENST00000472292.1:n.166-803A>G
ENST00000486167.1:n.101-803A>G
NM_000577.4:c.63-803A>G NP_000568.1:n.63-803A>G
NM_173841.2:c.126-803A>G , LRG_188t1:c.126-803A>G NP_776213.1:n.126-803A>G
NM_173842.2:c.117-803A>G NP_776214.1:n.117-803A>G
NM_173843.2:c.15-803A>G NP_776215.1:n.15-803A>G
XM_005263661.3:c.15-803A>G XP_005263718.1:n.15-803A>G
XM_006712497.2:c.15-803A>G XP_006712560.1:n.15-803A>G
XM_011511121.1:c.15-803A>G XP_011509423.1:n.15-803A>G
NM_001318914.1:c.15-803A>G NP_001305843.1:n.15-803A>G
XM_005263661.4:c.15-803A>G XP_005263718.1:n.15-803A>G
NM_000577.5:c.63-803A>G NP_000568.1:n.63-803A>G
NM_001318914.2:c.15-803A>G NP_001305843.1:n.15-803A>G
NM_173842.3:c.117-803A>G MANE Select NP_776214.1:n.117-803A>G
NM_173843.3:c.15-803A>G NP_776215.1:n.15-803A>G
NM_001379360.1:c.15-803A>G NP_001366289.1:n.15-803A>G
NM_173841.3:c.126-803A>G NP_776213.1:n.126-803A>G