Canonical Allele Identifier: CA348296168

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113132767-T-C
• MyVariant Identifiers: chr2:g.113890344T>C (hg19) ; chr2:g.113132767T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132767T>C , CM000664.2:g.113132767T>C	GRCh38
NC_000002.11:g.113890344T>C , CM000664.1:g.113890344T>C	GRCh37
NC_000002.10:g.113606815T>C	NCBI36
NG_021240.1:g.19875T>C , LRG_188:g.19875T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.328T>C	ENSP00000387210.1:p.Trp110Arg
ENST00000696879.1:c.328T>C	ENSP00000512947.1:p.Trp110Arg
ENST00000696880.1:c.328T>C	ENSP00000512948.1:p.Trp110Arg
ENST00000696881.1:c.328T>C	ENSP00000512949.1:p.Trp110Arg
ENST00000696882.1:c.*200T>C	ENSP00000512950.1:n.*200T>C
ENST00000696883.1:n.375T>C
ENST00000409930.4:c.430T>C MANE Select	ENSP00000387173.3:p.Trp144Arg
ENST00000259206.9:c.439T>C	ENSP00000259206.5:p.Trp147Arg
ENST00000354115.6:c.376T>C	ENSP00000329072.3:p.Trp126Arg
ENST00000361779.7:c.328T>C	ENSP00000354816.3:p.Trp110Arg
ENST00000409052.5:c.328T>C	ENSP00000387210.1:p.Trp110Arg
ENST00000409930.3:c.430T>C	ENSP00000387173.3:p.Trp144Arg
NM_000577.4:c.376T>C	NP_000568.1:p.Trp126Arg
NM_173841.2:c.439T>C , LRG_188t1:c.439T>C	NP_776213.1:p.Trp147Arg
NM_173842.2:c.430T>C	NP_776214.1:p.Trp144Arg
NM_173843.2:c.328T>C	NP_776215.1:p.Trp110Arg
XM_005263661.3:c.328T>C	XP_005263718.1:p.Trp110Arg
XM_006712497.2:c.328T>C	XP_006712560.1:p.Trp110Arg
XM_011511121.1:c.328T>C	XP_011509423.1:p.Trp110Arg
NM_001318914.1:c.328T>C	NP_001305843.1:p.Trp110Arg
XM_005263661.4:c.328T>C	XP_005263718.1:p.Trp110Arg
NM_000577.5:c.376T>C	NP_000568.1:p.Trp126Arg
NM_001318914.2:c.328T>C	NP_001305843.1:p.Trp110Arg
NM_173842.3:c.430T>C MANE Select	NP_776214.1:p.Trp144Arg
NM_173843.3:c.328T>C	NP_776215.1:p.Trp110Arg
NM_001379360.1:c.328T>C	NP_001366289.1:p.Trp110Arg
NM_173841.3:c.439T>C	NP_776213.1:p.Trp147Arg