Canonical Allele Identifier: CA2751751131

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133270_113133277del , CM000664.2:g.113133270_113133277del	GRCh38
NC_000002.11:g.113890847_113890854del , CM000664.1:g.113890847_113890854del	GRCh37
NC_000002.10:g.113607318_113607325del	NCBI36
NG_021240.1:g.20378_20385del , LRG_188:g.20378_20385del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*399_*406del	ENSP00000387210.1:n.*399_*406del
ENST00000696879.1:c.*399_*406del	ENSP00000512947.1:n.*399_*406del
ENST00000696880.1:c.*212-95_*212-88del	ENSP00000512948.1:n.*212-95_*212-88del
ENST00000696882.1:c.*703_*710del	ENSP00000512950.1:n.*703_*710del
ENST00000409930.4:c.*399_*406del MANE Select	ENSP00000387173.3:n.*399_*406del
ENST00000259206.9:c.*399_*406del	ENSP00000259206.5:n.*399_*406del
ENST00000354115.6:c.*399_*406del	ENSP00000329072.3:n.*399_*406del
ENST00000361779.7:c.*399_*406del	ENSP00000354816.3:n.*399_*406del
ENST00000409052.5:c.*399_*406del	ENSP00000387210.1:n.*399_*406del
NM_000577.4:c.*399_*406del	NP_000568.1:n.*399_*406del
NM_173841.2:c.*399_*406del , LRG_188t1:c.*399_*406del	NP_776213.1:n.*399_*406del
NM_173842.2:c.*399_*406del	NP_776214.1:n.*399_*406del
NM_173843.2:c.*399_*406del	NP_776215.1:n.*399_*406del
XM_005263661.3:c.*399_*406del	XP_005263718.1:n.*399_*406del
XM_006712497.2:c.*399_*406del	XP_006712560.1:n.*399_*406del
XM_011511121.1:c.*399_*406del	XP_011509423.1:n.*399_*406del
NM_001318914.1:c.*399_*406del	NP_001305843.1:n.*399_*406del
XM_005263661.4:c.*399_*406del	XP_005263718.1:n.*399_*406del
NM_000577.5:c.*399_*406del	NP_000568.1:n.*399_*406del
NM_001318914.2:c.*399_*406del	NP_001305843.1:n.*399_*406del
NM_173842.3:c.*399_*406del MANE Select	NP_776214.1:n.*399_*406del
NM_173843.3:c.*399_*406del	NP_776215.1:n.*399_*406del
NM_001379360.1:c.*399_*406del	NP_001366289.1:n.*399_*406del
NM_173841.3:c.*399_*406del	NP_776213.1:n.*399_*406del