Canonical Allele Identifier: CA1035147403

Gene: IL1RN

Linked Data

• dbSNP Id: rs1686789178
• gnomAD v3: 2-113121745-T-TG
• gnomAD v4: 2-113121745-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113121750dup , CM000664.2:g.113121750dup	GRCh38
NC_000002.11:g.113879327dup , CM000664.1:g.113879327dup	GRCh37
NC_000002.10:g.113595798dup	NCBI36
NG_021240.1:g.8858dup , LRG_188:g.8858dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-39+132dup	ENSP00000387210.1:n.-39+132dup
ENST00000696881.1:c.-39+132dup	ENSP00000512949.1:n.-39+132dup
ENST00000259206.9:c.73+1622dup	ENSP00000259206.5:n.73+1622dup
ENST00000354115.6:c.10+3722dup	ENSP00000329072.3:n.10+3722dup
ENST00000361779.7:c.-39+132dup	ENSP00000354816.3:n.-39+132dup
ENST00000409052.5:c.-39+132dup	ENSP00000387210.1:n.-39+132dup
ENST00000486167.1:n.48+3722dup
NM_000577.4:c.10+3722dup	NP_000568.1:n.10+3722dup
NM_173841.2:c.73+1622dup , LRG_188t1:c.73+1622dup	NP_776213.1:n.73+1622dup
NM_173843.2:c.-39+132dup	NP_776215.1:n.-39+132dup
XM_006712497.2:c.-39+132dup	XP_006712560.1:n.-39+132dup
XM_011511121.1:c.-39+132dup	XP_011509423.1:n.-39+132dup
NM_001318914.1:c.-39+132dup	NP_001305843.1:n.-39+132dup
NM_000577.5:c.10+3722dup	NP_000568.1:n.10+3722dup
NM_001318914.2:c.-39+132dup	NP_001305843.1:n.-39+132dup
NM_173843.3:c.-39+132dup	NP_776215.1:n.-39+132dup
NM_173841.3:c.73+1622dup	NP_776213.1:n.73+1622dup