Canonical Allele Identifier: CA1742563531

Gene: IRF5

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128948646G= , CM000669.2:g.128948646G=	GRCh38
NC_000007.13:g.128588700G= , CM000669.1:g.128588700G=	GRCh37
NC_000007.12:g.128375936G=	NCBI36
NG_012306.1:g.15707G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700148.1:n.1609G=
ENST00000700151.1:n.3875G=
ENST00000700152.1:n.3415G=
ENST00000700153.1:n.2789G=
ENST00000700154.1:n.953G=
ENST00000357234.10:c.1373G= MANE Select	ENSP00000349770.5:p.Arg458=
ENST00000489702.6:c.1373G=	ENSP00000418037.2:p.Arg458=
ENST00000249375.8:c.1325G=	ENSP00000249375.4:p.Arg442=
ENST00000357234.9:c.1373G=	ENSP00000349770.5:p.Arg458=
ENST00000402030.6:c.1325G=	ENSP00000385352.2:p.Arg442=
ENST00000465603.5:c.*853G=	ENSP00000418534.1:n.*853G=
ENST00000473745.5:c.1325G=	ENSP00000419149.1:p.Arg442=
ENST00000477535.5:c.1067G=	ENSP00000419950.1:p.Arg356=
ENST00000619830.1:c.*823G=	ENSP00000483292.1:n.*823G=
NM_001098627.3:c.1325G=	NP_001092097.2:p.Arg442=
NM_001098629.2:c.1373G=	NP_001092099.1:p.Arg458=
NM_001098630.2:c.1325G=	NP_001092100.1:p.Arg442=
NM_001242452.2:c.1067G=	NP_001229381.1:p.Arg356=
NM_032643.4:c.1325G=	NP_116032.1:p.Arg442=
XM_005250317.2:c.1373G=	XP_005250374.1:p.Arg458=
XM_006715974.2:c.1373G=	XP_006716037.1:p.Arg458=
XM_011516158.1:c.1373G=	XP_011514460.1:p.Arg458=
XM_011516159.1:c.1373G=	XP_011514461.1:p.Arg458=
XM_011516160.1:c.1373G=	XP_011514462.1:p.Arg458=
XM_011516161.1:c.1343G=	XP_011514463.1:p.Arg448=
XM_011516162.1:c.1295G=	XP_011514464.1:p.Arg432=
XM_011516163.1:c.1295G=	XP_011514465.1:p.Arg432=
XM_011516164.1:c.1295G=	XP_011514466.1:p.Arg432=
NM_001347928.1:c.1373G=	NP_001334857.1:p.Arg458=
NM_001364314.1:c.1373G=	NP_001351243.1:p.Arg458=
XM_011516158.3:c.1373G=	XP_011514460.1:p.Arg458=
XM_011516159.3:c.1373G=	XP_011514461.1:p.Arg458=
NM_001098629.3:c.1373G= MANE Select	NP_001092099.1:p.Arg458=
NM_001098630.3:c.1325G=	NP_001092100.1:p.Arg442=
NM_001242452.3:c.1067G=	NP_001229381.1:p.Arg356=
NM_001347928.2:c.1373G=	NP_001334857.1:p.Arg458=
NM_001364314.2:c.1373G=	NP_001351243.1:p.Arg458=
NM_001098627.4:c.1325G=	NP_001092097.2:p.Arg442=
NM_032643.5:c.1325G=	NP_116032.1:p.Arg442=