Canonical Allele Identifier: CA2660766579

Gene: IL1RN

Linked Data

• gnomAD v4: 2-113133884-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113133884T>C , CM000664.2:g.113133884T>C	GRCh38
NC_000002.11:g.113891461T>C , CM000664.1:g.113891461T>C	GRCh37
NC_000002.10:g.113607932T>C	NCBI36
NG_021240.1:g.20992T>C , LRG_188:g.20992T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.*871T>C	ENSP00000387210.1:n.*871T>C
ENST00000696880.1:c.*550T>C	ENSP00000512948.1:n.*550T>C
ENST00000409930.4:c.*1013T>C MANE Select	ENSP00000387173.3:n.*1013T>C
ENST00000259206.9:c.*1013T>C	ENSP00000259206.5:n.*1013T>C
ENST00000354115.6:c.*1013T>C	ENSP00000329072.3:n.*1013T>C
ENST00000361779.7:c.*1013T>C	ENSP00000354816.3:n.*1013T>C
ENST00000409052.5:c.*871T>C	ENSP00000387210.1:n.*871T>C
NM_000577.4:c.*1013T>C	NP_000568.1:n.*1013T>C
NM_173841.2:c.*1013T>C , LRG_188t1:c.*1013T>C	NP_776213.1:n.*1013T>C
NM_173842.2:c.*1013T>C	NP_776214.1:n.*1013T>C
NM_173843.2:c.*1013T>C	NP_776215.1:n.*1013T>C
XM_005263661.3:c.*1013T>C	XP_005263718.1:n.*1013T>C
XM_006712497.2:c.*1013T>C	XP_006712560.1:n.*1013T>C
XM_011511121.1:c.*1013T>C	XP_011509423.1:n.*1013T>C
NM_001318914.1:c.*1013T>C	NP_001305843.1:n.*1013T>C
XM_005263661.4:c.*1013T>C	XP_005263718.1:n.*1013T>C
NM_000577.5:c.*1013T>C	NP_000568.1:n.*1013T>C
NM_001318914.2:c.*1013T>C	NP_001305843.1:n.*1013T>C
NM_173842.3:c.*1013T>C MANE Select	NP_776214.1:n.*1013T>C
NM_173843.3:c.*1013T>C	NP_776215.1:n.*1013T>C
NM_001379360.1:c.*1013T>C	NP_001366289.1:n.*1013T>C
NM_173841.3:c.*1013T>C	NP_776213.1:n.*1013T>C