Canonical Allele Identifier: CA428554431

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113132709-C-T
• MyVariant Identifiers: chr2:g.113890286C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132709C>T , CM000664.2:g.113132709C>T	GRCh38
NC_000002.11:g.113890286C>T , CM000664.1:g.113890286C>T	GRCh37
NC_000002.10:g.113606757C>T	NCBI36
NG_021240.1:g.19817C>T , LRG_188:g.19817C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.270C>T	ENSP00000387210.1:p.Ala90=
ENST00000696879.1:c.270C>T	ENSP00000512947.1:p.Ala90=
ENST00000696880.1:c.270C>T	ENSP00000512948.1:p.Ala90=
ENST00000696881.1:c.270C>T	ENSP00000512949.1:p.Ala90=
ENST00000696882.1:c.*142C>T	ENSP00000512950.1:n.*142C>T
ENST00000696883.1:n.317C>T
ENST00000409930.4:c.372C>T MANE Select	ENSP00000387173.3:p.Ala124=
ENST00000259206.9:c.381C>T	ENSP00000259206.5:p.Ala127=
ENST00000354115.6:c.318C>T	ENSP00000329072.3:p.Ala106=
ENST00000361779.7:c.270C>T	ENSP00000354816.3:p.Ala90=
ENST00000409052.5:c.270C>T	ENSP00000387210.1:p.Ala90=
ENST00000409930.3:c.372C>T	ENSP00000387173.3:p.Ala124=
NM_000577.4:c.318C>T	NP_000568.1:p.Ala106=
NM_173841.2:c.381C>T , LRG_188t1:c.381C>T	NP_776213.1:p.Ala127=
NM_173842.2:c.372C>T	NP_776214.1:p.Ala124=
NM_173843.2:c.270C>T	NP_776215.1:p.Ala90=
XM_005263661.3:c.270C>T	XP_005263718.1:p.Ala90=
XM_006712497.2:c.270C>T	XP_006712560.1:p.Ala90=
XM_011511121.1:c.270C>T	XP_011509423.1:p.Ala90=
NM_001318914.1:c.270C>T	NP_001305843.1:p.Ala90=
XM_005263661.4:c.270C>T	XP_005263718.1:p.Ala90=
NM_000577.5:c.318C>T	NP_000568.1:p.Ala106=
NM_001318914.2:c.270C>T	NP_001305843.1:p.Ala90=
NM_173842.3:c.372C>T MANE Select	NP_776214.1:p.Ala124=
NM_173843.3:c.270C>T	NP_776215.1:p.Ala90=
NM_001379360.1:c.270C>T	NP_001366289.1:p.Ala90=
NM_173841.3:c.381C>T	NP_776213.1:p.Ala127=