Canonical Allele Identifier: CA348296192

Gene: IL1RN

Linked Data

• MyVariant Identifiers: chr2:g.113890354G>C (hg19) ; chr2:g.113132777G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132777G>C , CM000664.2:g.113132777G>C	GRCh38
NC_000002.11:g.113890354G>C , CM000664.1:g.113890354G>C	GRCh37
NC_000002.10:g.113606825G>C	NCBI36
NG_021240.1:g.19885G>C , LRG_188:g.19885G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.338G>C	ENSP00000387210.1:p.Cys113Ser
ENST00000696879.1:c.338G>C	ENSP00000512947.1:p.Cys113Ser
ENST00000696880.1:c.338G>C	ENSP00000512948.1:p.Cys113Ser
ENST00000696881.1:c.338G>C	ENSP00000512949.1:p.Cys113Ser
ENST00000696882.1:c.*210G>C	ENSP00000512950.1:n.*210G>C
ENST00000696883.1:n.385G>C
ENST00000409930.4:c.440G>C MANE Select	ENSP00000387173.3:p.Cys147Ser
ENST00000259206.9:c.449G>C	ENSP00000259206.5:p.Cys150Ser
ENST00000354115.6:c.386G>C	ENSP00000329072.3:p.Cys129Ser
ENST00000361779.7:c.338G>C	ENSP00000354816.3:p.Cys113Ser
ENST00000409052.5:c.338G>C	ENSP00000387210.1:p.Cys113Ser
ENST00000409930.3:c.440G>C	ENSP00000387173.3:p.Cys147Ser
NM_000577.4:c.386G>C	NP_000568.1:p.Cys129Ser
NM_173841.2:c.449G>C , LRG_188t1:c.449G>C	NP_776213.1:p.Cys150Ser
NM_173842.2:c.440G>C	NP_776214.1:p.Cys147Ser
NM_173843.2:c.338G>C	NP_776215.1:p.Cys113Ser
XM_005263661.3:c.338G>C	XP_005263718.1:p.Cys113Ser
XM_006712497.2:c.338G>C	XP_006712560.1:p.Cys113Ser
XM_011511121.1:c.338G>C	XP_011509423.1:p.Cys113Ser
NM_001318914.1:c.338G>C	NP_001305843.1:p.Cys113Ser
XM_005263661.4:c.338G>C	XP_005263718.1:p.Cys113Ser
NM_000577.5:c.386G>C	NP_000568.1:p.Cys129Ser
NM_001318914.2:c.338G>C	NP_001305843.1:p.Cys113Ser
NM_173842.3:c.440G>C MANE Select	NP_776214.1:p.Cys147Ser
NM_173843.3:c.338G>C	NP_776215.1:p.Cys113Ser
NM_001379360.1:c.338G>C	NP_001366289.1:p.Cys113Ser
NM_173841.3:c.449G>C	NP_776213.1:p.Cys150Ser