Canonical Allele Identifier: CA2521062951

Gene: IL1RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113121589_113121590insCTTTG , CM000664.2:g.113121589_113121590insCTTTG	GRCh38
NC_000002.11:g.113879166_113879167insCTTTG , CM000664.1:g.113879166_113879167insCTTTG	GRCh37
NC_000002.10:g.113595637_113595638insCTTTG	NCBI36
NG_021240.1:g.8697_8698insCTTTG , LRG_188:g.8697_8698insCTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-68_-67insCTTTG	ENSP00000387210.1:n.-68_-67insCTTTG
ENST00000696881.1:c.-68_-67insCTTTG	ENSP00000512949.1:n.-68_-67insCTTTG
ENST00000259206.9:c.73+1461_73+1462insCTTTG	ENSP00000259206.5:n.73+1461_73+1462insCTTTG
ENST00000354115.6:c.10+3561_10+3562insCTTTG	ENSP00000329072.3:n.10+3561_10+3562insCTTTG
ENST00000361779.7:c.-68_-67insCTTTG	ENSP00000354816.3:n.-68_-67insCTTTG
ENST00000409052.5:c.-68_-67insCTTTG	ENSP00000387210.1:n.-68_-67insCTTTG
ENST00000486167.1:n.48+3561_48+3562insCTTTG
NM_000577.4:c.10+3561_10+3562insCTTTG	NP_000568.1:n.10+3561_10+3562insCTTTG
NM_173841.2:c.73+1461_73+1462insCTTTG , LRG_188t1:c.73+1461_73+1462insCTTTG	NP_776213.1:n.73+1461_73+1462insCTTTG
NM_173843.2:c.-68_-67insCTTTG	NP_776215.1:n.-68_-67insCTTTG
XM_006712497.2:c.-68_-67insCTTTG	XP_006712560.1:n.-68_-67insCTTTG
XM_011511121.1:c.-68_-67insCTTTG	XP_011509423.1:n.-68_-67insCTTTG
NM_001318914.1:c.-68_-67insCTTTG	NP_001305843.1:n.-68_-67insCTTTG
NM_000577.5:c.10+3561_10+3562insCTTTG	NP_000568.1:n.10+3561_10+3562insCTTTG
NM_001318914.2:c.-68_-67insCTTTG	NP_001305843.1:n.-68_-67insCTTTG
NM_173843.3:c.-68_-67insCTTTG	NP_776215.1:n.-68_-67insCTTTG
NM_173841.3:c.73+1461_73+1462insCTTTG	NP_776213.1:n.73+1461_73+1462insCTTTG