Canonical Allele Identifier: CA348292120

Gene: IL1RN

Linked Data

• COSMIC: COSM3565484
• MyVariant Identifiers: chr2:g.113875605G>A (hg19) ; chr2:g.113118028G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113118028G>A , CM000664.2:g.113118028G>A	GRCh38
NC_000002.11:g.113875605G>A , CM000664.1:g.113875605G>A	GRCh37
NC_000002.10:g.113592076G>A	NCBI36
NG_021240.1:g.5136G>A , LRG_188:g.5136G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2038G>A	ENSP00000387210.1:n.-272-2038G>A
ENST00000465812.6:n.775+363G>A
ENST00000696881.1:c.-273G>A	ENSP00000512949.1:n.-273G>A
ENST00000259206.9:c.10G>A	ENSP00000259206.5:p.Ala4Thr
ENST00000354115.6:c.10G>A	ENSP00000329072.3:p.Glu4Lys
ENST00000361779.7:c.-210G>A	ENSP00000354816.3:n.-210G>A
ENST00000409052.5:c.-272-2038G>A	ENSP00000387210.1:n.-272-2038G>A
ENST00000486167.1:n.48G>A
NM_000577.4:c.10G>A	NP_000568.1:p.Glu4Lys
NM_173841.2:c.10G>A , LRG_188t1:c.10G>A	NP_776213.1:p.Ala4Thr
NM_173843.2:c.-210G>A	NP_776215.1:n.-210G>A
XM_006712497.2:c.-273G>A	XP_006712560.1:n.-273G>A
XM_011511121.1:c.-272-2038G>A	XP_011509423.1:n.-272-2038G>A
NM_001318914.1:c.-273G>A	NP_001305843.1:n.-273G>A
NM_000577.5:c.10G>A	NP_000568.1:p.Glu4Lys
NM_001318914.2:c.-273G>A	NP_001305843.1:n.-273G>A
NM_173843.3:c.-210G>A	NP_776215.1:n.-210G>A
NM_173841.3:c.10G>A	NP_776213.1:p.Ala4Thr