Canonical Allele Identifier: CA2660763986

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113118014-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113118018del , CM000664.2:g.113118018del	GRCh38
NC_000002.11:g.113875595del , CM000664.1:g.113875595del	GRCh37
NC_000002.10:g.113592066del	NCBI36
NG_021240.1:g.5126del , LRG_188:g.5126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2048del	ENSP00000387210.1:n.-272-2048del
ENST00000465812.6:n.775+353del
ENST00000696881.1:c.-283del	ENSP00000512949.1:n.-283del
ENST00000259206.9:c.-1del	ENSP00000259206.5:n.-1del
ENST00000354115.6:c.-1del	ENSP00000329072.3:n.-1del
ENST00000361779.7:c.-220del	ENSP00000354816.3:n.-220del
ENST00000409052.5:c.-272-2048del	ENSP00000387210.1:n.-272-2048del
ENST00000486167.1:n.38del
NM_000577.4:c.-1del	NP_000568.1:n.-1del
NM_173841.2:c.-1del , LRG_188t1:c.-1del	NP_776213.1:n.-1del
NM_173843.2:c.-220del	NP_776215.1:n.-220del
XM_006712497.2:c.-283del	XP_006712560.1:n.-283del
XM_011511121.1:c.-272-2048del	XP_011509423.1:n.-272-2048del
NM_001318914.1:c.-283del	NP_001305843.1:n.-283del
NM_000577.5:c.-1del	NP_000568.1:n.-1del
NM_001318914.2:c.-283del	NP_001305843.1:n.-283del
NM_173843.3:c.-220del	NP_776215.1:n.-220del
NM_173841.3:c.-1del	NP_776213.1:n.-1del