Canonical Allele Identifier: CA1280073820

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133793_113133794delinsCT , CM000664.2:g.113133793_113133794delinsCT	GRCh38
NC_000002.11:g.113891370_113891371delinsCT , CM000664.1:g.113891370_113891371delinsCT	GRCh37
NC_000002.10:g.113607841_113607842delinsCT	NCBI36
NG_021240.1:g.20901_20902delinsCT , LRG_188:g.20901_20902delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000409052.6:c.*780_*781delinsCT	ENSP00000387210.1:n.*780_*781delinsCT
ENST00000696880.1:c.*459_*460delinsCT	ENSP00000512948.1:n.*459_*460delinsCT
ENST00000409930.4:c.*922_*923delinsCT MANE Select	ENSP00000387173.3:n.*922_*923delinsCT
ENST00000259206.9:c.*922_*923delinsCT	ENSP00000259206.5:n.*922_*923delinsCT
ENST00000354115.6:c.*922_*923delinsCT	ENSP00000329072.3:n.*922_*923delinsCT
ENST00000361779.7:c.*922_*923delinsCT	ENSP00000354816.3:n.*922_*923delinsCT
ENST00000409052.5:c.*780_*781delinsCT	ENSP00000387210.1:n.*780_*781delinsCT
NM_000577.4:c.*922_*923delinsCT	NP_000568.1:n.*922_*923delinsCT
NM_173841.2:c.*922_*923delinsCT , LRG_188t1:c.*922_*923delinsCT	NP_776213.1:n.*922_*923delinsCT
NM_173842.2:c.*922_*923delinsCT	NP_776214.1:n.*922_*923delinsCT
NM_173843.2:c.*922_*923delinsCT	NP_776215.1:n.*922_*923delinsCT
XM_005263661.3:c.*922_*923delinsCT	XP_005263718.1:n.*922_*923delinsCT
XM_006712497.2:c.*922_*923delinsCT	XP_006712560.1:n.*922_*923delinsCT
XM_011511121.1:c.*922_*923delinsCT	XP_011509423.1:n.*922_*923delinsCT
NM_001318914.1:c.*922_*923delinsCT	NP_001305843.1:n.*922_*923delinsCT
XM_005263661.4:c.*922_*923delinsCT	XP_005263718.1:n.*922_*923delinsCT
NM_000577.5:c.*922_*923delinsCT	NP_000568.1:n.*922_*923delinsCT
NM_001318914.2:c.*922_*923delinsCT	NP_001305843.1:n.*922_*923delinsCT
NM_173842.3:c.*922_*923delinsCT MANE Select	NP_776214.1:n.*922_*923delinsCT
NM_173843.3:c.*922_*923delinsCT	NP_776215.1:n.*922_*923delinsCT
NM_001379360.1:c.*922_*923delinsCT	NP_001366289.1:n.*922_*923delinsCT
NM_173841.3:c.*922_*923delinsCT	NP_776213.1:n.*922_*923delinsCT