Canonical Allele Identifier: CA457847526
Gene: IRF5 HGNC NCBI

Linked Data

dbSNP Id: rs1585310487
MyVariant Identifiers: chr7:g.128588680T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128948626T>G , CM000669.2:g.128948626T>G GRCh38
NC_000007.13:g.128588680T>G , CM000669.1:g.128588680T>G GRCh37
NC_000007.12:g.128375916T>G NCBI36
NG_012306.1:g.15687T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700148.1:n.1589T>G
ENST00000700151.1:n.3855T>G
ENST00000700152.1:n.3395T>G
ENST00000700153.1:n.2769T>G
ENST00000700154.1:n.933T>G
ENST00000357234.10:c.1353T>G MANE Select ENSP00000349770.5:p.Ser451=
ENST00000489702.6:c.1353T>G ENSP00000418037.2:p.Ser451=
ENST00000249375.8:c.1305T>G ENSP00000249375.4:p.Ser435=
ENST00000357234.9:c.1353T>G ENSP00000349770.5:p.Ser451=
ENST00000402030.6:c.1305T>G ENSP00000385352.2:p.Ser435=
ENST00000465603.5:c.*833T>G ENSP00000418534.1:n.*833T>G
ENST00000473745.5:c.1305T>G ENSP00000419149.1:p.Ser435=
ENST00000477535.5:c.1047T>G ENSP00000419950.1:p.Ser349=
ENST00000619830.1:c.*803T>G ENSP00000483292.1:n.*803T>G
NM_001098627.3:c.1305T>G NP_001092097.2:p.Ser435=
NM_001098629.2:c.1353T>G NP_001092099.1:p.Ser451=
NM_001098630.2:c.1305T>G NP_001092100.1:p.Ser435=
NM_001242452.2:c.1047T>G NP_001229381.1:p.Ser349=
NM_032643.4:c.1305T>G NP_116032.1:p.Ser435=
XM_005250317.2:c.1353T>G XP_005250374.1:p.Ser451=
XM_006715974.2:c.1353T>G XP_006716037.1:p.Ser451=
XM_011516158.1:c.1353T>G XP_011514460.1:p.Ser451=
XM_011516159.1:c.1353T>G XP_011514461.1:p.Ser451=
XM_011516160.1:c.1353T>G XP_011514462.1:p.Ser451=
XM_011516161.1:c.1323T>G XP_011514463.1:p.Ser441=
XM_011516162.1:c.1275T>G XP_011514464.1:p.Ser425=
XM_011516163.1:c.1275T>G XP_011514465.1:p.Ser425=
XM_011516164.1:c.1275T>G XP_011514466.1:p.Ser425=
NM_001347928.1:c.1353T>G NP_001334857.1:p.Ser451=
NM_001364314.1:c.1353T>G NP_001351243.1:p.Ser451=
XM_011516158.3:c.1353T>G XP_011514460.1:p.Ser451=
XM_011516159.3:c.1353T>G XP_011514461.1:p.Ser451=
NM_001098629.3:c.1353T>G MANE Select NP_001092099.1:p.Ser451=
NM_001098630.3:c.1305T>G NP_001092100.1:p.Ser435=
NM_001242452.3:c.1047T>G NP_001229381.1:p.Ser349=
NM_001347928.2:c.1353T>G NP_001334857.1:p.Ser451=
NM_001364314.2:c.1353T>G NP_001351243.1:p.Ser451=
NM_001098627.4:c.1305T>G NP_001092097.2:p.Ser435=
NM_032643.5:c.1305T>G NP_116032.1:p.Ser435=