Canonical Allele Identifier: CA1280071925

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113129685C= , CM000664.2:g.113129685C=	GRCh38
NC_000002.11:g.113887262C= , CM000664.1:g.113887262C=	GRCh37
NC_000002.10:g.113603733C=	NCBI36
NG_021240.1:g.16793C= , LRG_188:g.16793C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.103+21C=	ENSP00000387210.1:n.103+21C=
ENST00000696879.1:c.103+21C=	ENSP00000512947.1:n.103+21C=
ENST00000696880.1:c.103+21C=	ENSP00000512948.1:n.103+21C=
ENST00000696881.1:c.103+21C=	ENSP00000512949.1:n.103+21C=
ENST00000696882.1:c.103+21C=	ENSP00000512950.1:n.103+21C=
ENST00000409930.4:c.205+21C= MANE Select	ENSP00000387173.3:n.205+21C=
ENST00000259206.9:c.214+21C=	ENSP00000259206.5:n.214+21C=
ENST00000354115.6:c.151+21C=	ENSP00000329072.3:n.151+21C=
ENST00000361779.7:c.103+21C=	ENSP00000354816.3:n.103+21C=
ENST00000409052.5:c.103+21C=	ENSP00000387210.1:n.103+21C=
ENST00000409930.3:c.205+21C=	ENSP00000387173.3:n.205+21C=
ENST00000472292.1:n.275C=
ENST00000486167.1:n.210C=
NM_000577.4:c.151+21C=	NP_000568.1:n.151+21C=
NM_173841.2:c.214+21C= , LRG_188t1:c.214+21C=	NP_776213.1:n.214+21C=
NM_173842.2:c.205+21C=	NP_776214.1:n.205+21C=
NM_173843.2:c.103+21C=	NP_776215.1:n.103+21C=
XM_005263661.3:c.103+21C=	XP_005263718.1:n.103+21C=
XM_006712497.2:c.103+21C=	XP_006712560.1:n.103+21C=
XM_011511121.1:c.103+21C=	XP_011509423.1:n.103+21C=
NM_001318914.1:c.103+21C=	NP_001305843.1:n.103+21C=
XM_005263661.4:c.103+21C=	XP_005263718.1:n.103+21C=
NM_000577.5:c.151+21C=	NP_000568.1:n.151+21C=
NM_001318914.2:c.103+21C=	NP_001305843.1:n.103+21C=
NM_173842.3:c.205+21C= MANE Select	NP_776214.1:n.205+21C=
NM_173843.3:c.103+21C=	NP_776215.1:n.103+21C=
NM_001379360.1:c.103+21C=	NP_001366289.1:n.103+21C=
NM_173841.3:c.214+21C=	NP_776213.1:n.214+21C=