Canonical Allele Identifier: CA369240772

Gene: IRF5

Linked Data

• dbSNP Id: rs1368490077
• gnomAD v2: 7-128588699-C-T
• gnomAD v4: 7-128948645-C-T
• MyVariant Identifiers: chr7:g.128588699C>T (hg19) ; chr7:g.128948645C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128948645C>T , CM000669.2:g.128948645C>T	GRCh38
NC_000007.13:g.128588699C>T , CM000669.1:g.128588699C>T	GRCh37
NC_000007.12:g.128375935C>T	NCBI36
NG_012306.1:g.15706C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700148.1:n.1608C>T
ENST00000700151.1:n.3874C>T
ENST00000700152.1:n.3414C>T
ENST00000700153.1:n.2788C>T
ENST00000700154.1:n.952C>T
ENST00000357234.10:c.1372C>T MANE Select	ENSP00000349770.5:p.Arg458Trp
ENST00000489702.6:c.1372C>T	ENSP00000418037.2:p.Arg458Trp
ENST00000249375.8:c.1324C>T	ENSP00000249375.4:p.Arg442Trp
ENST00000357234.9:c.1372C>T	ENSP00000349770.5:p.Arg458Trp
ENST00000402030.6:c.1324C>T	ENSP00000385352.2:p.Arg442Trp
ENST00000465603.5:c.*852C>T	ENSP00000418534.1:n.*852C>T
ENST00000473745.5:c.1324C>T	ENSP00000419149.1:p.Arg442Trp
ENST00000477535.5:c.1066C>T	ENSP00000419950.1:p.Arg356Trp
ENST00000619830.1:c.*822C>T	ENSP00000483292.1:n.*822C>T
NM_001098627.3:c.1324C>T	NP_001092097.2:p.Arg442Trp
NM_001098629.2:c.1372C>T	NP_001092099.1:p.Arg458Trp
NM_001098630.2:c.1324C>T	NP_001092100.1:p.Arg442Trp
NM_001242452.2:c.1066C>T	NP_001229381.1:p.Arg356Trp
NM_032643.4:c.1324C>T	NP_116032.1:p.Arg442Trp
XM_005250317.2:c.1372C>T	XP_005250374.1:p.Arg458Trp
XM_006715974.2:c.1372C>T	XP_006716037.1:p.Arg458Trp
XM_011516158.1:c.1372C>T	XP_011514460.1:p.Arg458Trp
XM_011516159.1:c.1372C>T	XP_011514461.1:p.Arg458Trp
XM_011516160.1:c.1372C>T	XP_011514462.1:p.Arg458Trp
XM_011516161.1:c.1342C>T	XP_011514463.1:p.Arg448Trp
XM_011516162.1:c.1294C>T	XP_011514464.1:p.Arg432Trp
XM_011516163.1:c.1294C>T	XP_011514465.1:p.Arg432Trp
XM_011516164.1:c.1294C>T	XP_011514466.1:p.Arg432Trp
NM_001347928.1:c.1372C>T	NP_001334857.1:p.Arg458Trp
NM_001364314.1:c.1372C>T	NP_001351243.1:p.Arg458Trp
XM_011516158.3:c.1372C>T	XP_011514460.1:p.Arg458Trp
XM_011516159.3:c.1372C>T	XP_011514461.1:p.Arg458Trp
NM_001098629.3:c.1372C>T MANE Select	NP_001092099.1:p.Arg458Trp
NM_001098630.3:c.1324C>T	NP_001092100.1:p.Arg442Trp
NM_001242452.3:c.1066C>T	NP_001229381.1:p.Arg356Trp
NM_001347928.2:c.1372C>T	NP_001334857.1:p.Arg458Trp
NM_001364314.2:c.1372C>T	NP_001351243.1:p.Arg458Trp
NM_001098627.4:c.1324C>T	NP_001092097.2:p.Arg442Trp
NM_032643.5:c.1324C>T	NP_116032.1:p.Arg442Trp