Canonical Allele Identifier: CA755268770

Gene: IL1RN

Linked Data

• dbSNP Id: rs1234289014
• MyVariant Identifiers: chr2:g.113875556_113875565del (hg19) ; chr2:g.113117979_113117988del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113117988_113117997del , CM000664.2:g.113117988_113117997del	GRCh38
NC_000002.11:g.113875565_113875574del , CM000664.1:g.113875565_113875574del	GRCh37
NC_000002.10:g.113592036_113592045del	NCBI36
NG_021240.1:g.5096_5105del , LRG_188:g.5096_5105del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.-272-2078_-272-2069del	ENSP00000387210.1:n.-272-2078_-272-2069del
ENST00000465812.6:n.775+323_775+332del
ENST00000696881.1:c.-313_-304del	ENSP00000512949.1:n.-313_-304del
ENST00000259206.9:c.-31_-22del	ENSP00000259206.5:n.-31_-22del
ENST00000354115.6:c.-31_-22del	ENSP00000329072.3:n.-31_-22del
ENST00000361779.7:c.-250_-241del	ENSP00000354816.3:n.-250_-241del
ENST00000409052.5:c.-272-2078_-272-2069del	ENSP00000387210.1:n.-272-2078_-272-2069del
NM_000577.4:c.-31_-22del	NP_000568.1:n.-31_-22del
NM_173841.2:c.-31_-22del , LRG_188t1:c.-31_-22del	NP_776213.1:n.-31_-22del
NM_173843.2:c.-250_-241del	NP_776215.1:n.-250_-241del
XM_006712497.2:c.-313_-304del	XP_006712560.1:n.-313_-304del
XM_011511121.1:c.-272-2078_-272-2069del	XP_011509423.1:n.-272-2078_-272-2069del
NM_001318914.1:c.-313_-304del	NP_001305843.1:n.-313_-304del
NM_000577.5:c.-31_-22del	NP_000568.1:n.-31_-22del
NM_001318914.2:c.-313_-304del	NP_001305843.1:n.-313_-304del
NM_173843.3:c.-250_-241del	NP_776215.1:n.-250_-241del
NM_173841.3:c.-31_-22del	NP_776213.1:n.-31_-22del