Canonical Allele Identifier: CA348296178

Gene: IL1RN

Linked Data

• MyVariant Identifiers: chr2:g.113890348T>C (hg19) ; chr2:g.113132771T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113132771T>C , CM000664.2:g.113132771T>C	GRCh38
NC_000002.11:g.113890348T>C , CM000664.1:g.113890348T>C	GRCh37
NC_000002.10:g.113606819T>C	NCBI36
NG_021240.1:g.19879T>C , LRG_188:g.19879T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409052.6:c.332T>C	ENSP00000387210.1:p.Phe111Ser
ENST00000696879.1:c.332T>C	ENSP00000512947.1:p.Phe111Ser
ENST00000696880.1:c.332T>C	ENSP00000512948.1:p.Phe111Ser
ENST00000696881.1:c.332T>C	ENSP00000512949.1:p.Phe111Ser
ENST00000696882.1:c.*204T>C	ENSP00000512950.1:n.*204T>C
ENST00000696883.1:n.379T>C
ENST00000409930.4:c.434T>C MANE Select	ENSP00000387173.3:p.Phe145Ser
ENST00000259206.9:c.443T>C	ENSP00000259206.5:p.Phe148Ser
ENST00000354115.6:c.380T>C	ENSP00000329072.3:p.Phe127Ser
ENST00000361779.7:c.332T>C	ENSP00000354816.3:p.Phe111Ser
ENST00000409052.5:c.332T>C	ENSP00000387210.1:p.Phe111Ser
ENST00000409930.3:c.434T>C	ENSP00000387173.3:p.Phe145Ser
NM_000577.4:c.380T>C	NP_000568.1:p.Phe127Ser
NM_173841.2:c.443T>C , LRG_188t1:c.443T>C	NP_776213.1:p.Phe148Ser
NM_173842.2:c.434T>C	NP_776214.1:p.Phe145Ser
NM_173843.2:c.332T>C	NP_776215.1:p.Phe111Ser
XM_005263661.3:c.332T>C	XP_005263718.1:p.Phe111Ser
XM_006712497.2:c.332T>C	XP_006712560.1:p.Phe111Ser
XM_011511121.1:c.332T>C	XP_011509423.1:p.Phe111Ser
NM_001318914.1:c.332T>C	NP_001305843.1:p.Phe111Ser
XM_005263661.4:c.332T>C	XP_005263718.1:p.Phe111Ser
NM_000577.5:c.380T>C	NP_000568.1:p.Phe127Ser
NM_001318914.2:c.332T>C	NP_001305843.1:p.Phe111Ser
NM_173842.3:c.434T>C MANE Select	NP_776214.1:p.Phe145Ser
NM_173843.3:c.332T>C	NP_776215.1:p.Phe111Ser
NM_001379360.1:c.332T>C	NP_001366289.1:p.Phe111Ser
NM_173841.3:c.443T>C	NP_776213.1:p.Phe148Ser