Canonical Allele Identifier: CA348296199

Gene: IL1RN

Linked Data

• MyVariant Identifiers: chr2:g.113890357C>A (hg19) ; chr2:g.113132780C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132780C>A , CM000664.2:g.113132780C>A	GRCh38
NC_000002.11:g.113890357C>A , CM000664.1:g.113890357C>A	GRCh37
NC_000002.10:g.113606828C>A	NCBI36
NG_021240.1:g.19888C>A , LRG_188:g.19888C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.341C>A	ENSP00000387210.1:p.Thr114Lys
ENST00000696879.1:c.341C>A	ENSP00000512947.1:p.Thr114Lys
ENST00000696880.1:c.341C>A	ENSP00000512948.1:p.Thr114Lys
ENST00000696881.1:c.341C>A	ENSP00000512949.1:p.Thr114Lys
ENST00000696882.1:c.*213C>A	ENSP00000512950.1:n.*213C>A
ENST00000696883.1:n.388C>A
ENST00000409930.4:c.443C>A MANE Select	ENSP00000387173.3:p.Thr148Lys
ENST00000259206.9:c.452C>A	ENSP00000259206.5:p.Thr151Lys
ENST00000354115.6:c.389C>A	ENSP00000329072.3:p.Thr130Lys
ENST00000361779.7:c.341C>A	ENSP00000354816.3:p.Thr114Lys
ENST00000409052.5:c.341C>A	ENSP00000387210.1:p.Thr114Lys
ENST00000409930.3:c.443C>A	ENSP00000387173.3:p.Thr148Lys
NM_000577.4:c.389C>A	NP_000568.1:p.Thr130Lys
NM_173841.2:c.452C>A , LRG_188t1:c.452C>A	NP_776213.1:p.Thr151Lys
NM_173842.2:c.443C>A	NP_776214.1:p.Thr148Lys
NM_173843.2:c.341C>A	NP_776215.1:p.Thr114Lys
XM_005263661.3:c.341C>A	XP_005263718.1:p.Thr114Lys
XM_006712497.2:c.341C>A	XP_006712560.1:p.Thr114Lys
XM_011511121.1:c.341C>A	XP_011509423.1:p.Thr114Lys
NM_001318914.1:c.341C>A	NP_001305843.1:p.Thr114Lys
XM_005263661.4:c.341C>A	XP_005263718.1:p.Thr114Lys
NM_000577.5:c.389C>A	NP_000568.1:p.Thr130Lys
NM_001318914.2:c.341C>A	NP_001305843.1:p.Thr114Lys
NM_173842.3:c.443C>A MANE Select	NP_776214.1:p.Thr148Lys
NM_173843.3:c.341C>A	NP_776215.1:p.Thr114Lys
NM_001379360.1:c.341C>A	NP_001366289.1:p.Thr114Lys
NM_173841.3:c.452C>A	NP_776213.1:p.Thr151Lys