Canonical Allele Identifier: CA2825000992

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113127670del , CM000664.2:g.113127670del	GRCh38
NC_000002.11:g.113885247del , CM000664.1:g.113885247del	GRCh37
NC_000002.10:g.113601718del	NCBI36
NG_021240.1:g.14778del , LRG_188:g.14778del

Transcript Alleles

HGVS	Amino-acid Change
NM_173842.3:c.46del MANE Select	NP_776214.1:p.Leu16SerfsTer?
ENST00000409930.4:c.46del MANE Select	ENSP00000387173.3:p.Leu16SerfsTer?
NM_000577.4:c.11-19del	NP_000568.1:n.11-19del
NM_000577.5:c.11-19del	NP_000568.1:n.11-19del
NM_001318914.1:c.-38-19del	NP_001305843.1:n.-38-19del
NM_001318914.2:c.-38-19del	NP_001305843.1:n.-38-19del
NM_001379360.1:c.-38-19del	NP_001366289.1:n.-38-19del
NM_173841.2:c.74-19del , LRG_188t1:c.74-19del	NP_776213.1:n.74-19del
NM_173841.3:c.74-19del	NP_776213.1:n.74-19del
NM_173842.2:c.46del	NP_776214.1:p.Leu16SerfsTer?
NM_173843.2:c.-38-19del	NP_776215.1:n.-38-19del
NM_173843.3:c.-38-19del	NP_776215.1:n.-38-19del
ENST00000259206.9:c.74-19del	ENSP00000259206.5:n.74-19del
ENST00000354115.6:c.11-19del	ENSP00000329072.3:n.11-19del
ENST00000361779.7:c.-38-19del	ENSP00000354816.3:n.-38-19del
ENST00000409052.5:c.-38-19del	ENSP00000387210.1:n.-38-19del
ENST00000409052.6:c.-38-19del	ENSP00000387210.1:n.-38-19del
ENST00000409930.3:c.46del	ENSP00000387173.3:p.Leu16SerfsTer?
ENST00000472292.1:n.95del
ENST00000486167.1:n.49-19del
ENST00000696879.1:c.-38-19del	ENSP00000512947.1:n.-38-19del
ENST00000696881.1:c.-38-19del	ENSP00000512949.1:n.-38-19del
ENST00000696882.1:c.-57del	ENSP00000512950.1:n.-57del
XM_005263661.3:c.-38-19del	XP_005263718.1:n.-38-19del
XM_005263661.4:c.-38-19del	XP_005263718.1:n.-38-19del
XM_006712497.2:c.-38-19del	XP_006712560.1:n.-38-19del
XM_011511121.1:c.-38-19del	XP_011509423.1:n.-38-19del