Canonical Allele Identifier: CA348292601

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113120080G>T , CM000664.2:g.113120080G>T	GRCh38
NC_000002.11:g.113877657G>T , CM000664.1:g.113877657G>T	GRCh37
NC_000002.10:g.113594128G>T	NCBI36
NG_021240.1:g.7188G>T , LRG_188:g.7188G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000577.4:c.10+2052G>T	NP_000568.1:n.10+2052G>T
NM_000577.5:c.10+2052G>T	NP_000568.1:n.10+2052G>T
NM_001318914.1:c.-258G>T	NP_001305843.1:n.-258G>T
NM_001318914.2:c.-258G>T	NP_001305843.1:n.-258G>T
NM_173841.2:c.25G>T , LRG_188t1:c.25G>T	NP_776213.1:p.Glu9Ter
NM_173841.3:c.25G>T	NP_776213.1:p.Glu9Ter
NM_173843.2:c.-209-1368G>T	NP_776215.1:n.-209-1368G>T
NM_173843.3:c.-209-1368G>T	NP_776215.1:n.-209-1368G>T
ENST00000259206.9:c.25G>T	ENSP00000259206.5:p.Glu9Ter
ENST00000354115.6:c.10+2052G>T	ENSP00000329072.3:n.10+2052G>T
ENST00000361779.7:c.-209-1368G>T	ENSP00000354816.3:n.-209-1368G>T
ENST00000409052.5:c.-258G>T	ENSP00000387210.1:n.-258G>T
ENST00000409052.6:c.-258G>T	ENSP00000387210.1:n.-258G>T
ENST00000465812.6:n.790G>T
ENST00000486167.1:n.48+2052G>T
ENST00000696881.1:c.-258G>T	ENSP00000512949.1:n.-258G>T
XM_006712497.2:c.-258G>T	XP_006712560.1:n.-258G>T
XM_011511121.1:c.-258G>T	XP_011509423.1:n.-258G>T