Canonical Allele Identifier: CA428306474

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113129600C>G , CM000664.2:g.113129600C>G	GRCh38
NC_000002.11:g.113887177C>G , CM000664.1:g.113887177C>G	GRCh37
NC_000002.10:g.113603648C>G	NCBI36
NG_021240.1:g.16708C>G , LRG_188:g.16708C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_173842.3:c.141C>G MANE Select	NP_776214.1:p.Thr47=
ENST00000409930.4:c.141C>G MANE Select	ENSP00000387173.3:p.Thr47=
NM_000577.4:c.87C>G	NP_000568.1:p.Thr29=
NM_000577.5:c.87C>G	NP_000568.1:p.Thr29=
NM_001318914.1:c.39C>G	NP_001305843.1:p.Thr13=
NM_001318914.2:c.39C>G	NP_001305843.1:p.Thr13=
NM_001379360.1:c.39C>G	NP_001366289.1:p.Thr13=
NM_173841.2:c.150C>G , LRG_188t1:c.150C>G	NP_776213.1:p.Thr50=
NM_173841.3:c.150C>G	NP_776213.1:p.Thr50=
NM_173842.2:c.141C>G	NP_776214.1:p.Thr47=
NM_173843.2:c.39C>G	NP_776215.1:p.Thr13=
NM_173843.3:c.39C>G	NP_776215.1:p.Thr13=
ENST00000259206.9:c.150C>G	ENSP00000259206.5:p.Thr50=
ENST00000354115.6:c.87C>G	ENSP00000329072.3:p.Thr29=
ENST00000361779.7:c.39C>G	ENSP00000354816.3:p.Thr13=
ENST00000409052.5:c.39C>G	ENSP00000387210.1:p.Thr13=
ENST00000409052.6:c.39C>G	ENSP00000387210.1:p.Thr13=
ENST00000409930.3:c.141C>G	ENSP00000387173.3:p.Thr47=
ENST00000472292.1:n.190C>G
ENST00000486167.1:n.125C>G
ENST00000696879.1:c.39C>G	ENSP00000512947.1:p.Thr13=
ENST00000696880.1:c.39C>G	ENSP00000512948.1:p.Thr13=
ENST00000696881.1:c.39C>G	ENSP00000512949.1:p.Thr13=
ENST00000696882.1:c.39C>G	ENSP00000512950.1:p.Thr13=
XM_005263661.3:c.39C>G	XP_005263718.1:p.Thr13=
XM_005263661.4:c.39C>G	XP_005263718.1:p.Thr13=
XM_006712497.2:c.39C>G	XP_006712560.1:p.Thr13=
XM_011511121.1:c.39C>G	XP_011509423.1:p.Thr13=