Canonical Allele Identifier: CA1742563813

Gene: IRF5

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128948760_128948779delinsGAGCAGGCCTTGGTGTTGGC , CM000669.2:g.128948760_128948779delinsGAGCAGGCCTTGGTGTTGGC	GRCh38
NC_000007.13:g.128588814_128588833delinsGAGCAGGCCTTGGTGTTGGC , CM000669.1:g.128588814_128588833delinsGAGCAGGCCTTGGTGTTGGC	GRCh37
NC_000007.12:g.128376050_128376069delinsGAGCAGGCCTTGGTGTTGGC	NCBI36
NG_012306.1:g.15821_15840delinsGAGCAGGCCTTGGTGTTGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700148.1:n.1723_1742delinsGAGCAGGCCTTGGTGTTGGC
ENST00000700151.1:n.3989_4008delinsGAGCAGGCCTTGGTGTTGGC
ENST00000700152.1:n.3529_3548delinsGAGCAGGCCTTGGTGTTGGC
ENST00000700153.1:n.2903_2922delinsGAGCAGGCCTTGGTGTTGGC
ENST00000700154.1:n.1067_1086delinsGAGCAGGCCTTGGTGTTGGC
ENST00000357234.10:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC MANE Select	ENSP00000349770.5:p.Gly496=
ENST00000489702.6:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	ENSP00000418037.2:p.Gly496=
ENST00000249375.8:c.1439_1458delinsGAGCAGGCCTTGGTGTTGGC	ENSP00000249375.4:p.Gly480=
ENST00000357234.9:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	ENSP00000349770.5:p.Gly496=
ENST00000402030.6:c.1439_1458delinsGAGCAGGCCTTGGTGTTGGC	ENSP00000385352.2:p.Gly480=
ENST00000465603.5:c.*967_*986delinsGAGCAGGCCTTGGTGTTGGC	ENSP00000418534.1:n.*967_*986delinsGAGCAGGCCTTGGTGTTGGC
ENST00000473745.5:c.1439_1458delinsGAGCAGGCCTTGGTGTTGGC	ENSP00000419149.1:p.Gly480=
ENST00000477535.5:c.1181_1200delinsGAGCAGGCCTTGGTGTTGGC	ENSP00000419950.1:p.Gly394=
ENST00000619830.1:c.*937_*956delinsGAGCAGGCCTTGGTGTTGGC	ENSP00000483292.1:n.*937_*956delinsGAGCAGGCCTTGGTGTTGGC
NM_001098627.3:c.1439_1458delinsGAGCAGGCCTTGGTGTTGGC	NP_001092097.2:p.Gly480=
NM_001098629.2:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	NP_001092099.1:p.Gly496=
NM_001098630.2:c.1439_1458delinsGAGCAGGCCTTGGTGTTGGC	NP_001092100.1:p.Gly480=
NM_001242452.2:c.1181_1200delinsGAGCAGGCCTTGGTGTTGGC	NP_001229381.1:p.Gly394=
NM_032643.4:c.1439_1458delinsGAGCAGGCCTTGGTGTTGGC	NP_116032.1:p.Gly480=
XM_005250317.2:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	XP_005250374.1:p.Gly496=
XM_006715974.2:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	XP_006716037.1:p.Gly496=
XM_011516158.1:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	XP_011514460.1:p.Gly496=
XM_011516159.1:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	XP_011514461.1:p.Gly496=
XM_011516160.1:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	XP_011514462.1:p.Gly496=
XM_011516161.1:c.1457_1476delinsGAGCAGGCCTTGGTGTTGGC	XP_011514463.1:p.Gly486=
XM_011516162.1:c.1409_1428delinsGAGCAGGCCTTGGTGTTGGC	XP_011514464.1:p.Gly470=
XM_011516163.1:c.1409_1428delinsGAGCAGGCCTTGGTGTTGGC	XP_011514465.1:p.Gly470=
XM_011516164.1:c.1409_1428delinsGAGCAGGCCTTGGTGTTGGC	XP_011514466.1:p.Gly470=
NM_001347928.1:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	NP_001334857.1:p.Gly496=
NM_001364314.1:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	NP_001351243.1:p.Gly496=
XM_011516158.3:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	XP_011514460.1:p.Gly496=
XM_011516159.3:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	XP_011514461.1:p.Gly496=
NM_001098629.3:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC MANE Select	NP_001092099.1:p.Gly496=
NM_001098630.3:c.1439_1458delinsGAGCAGGCCTTGGTGTTGGC	NP_001092100.1:p.Gly480=
NM_001242452.3:c.1181_1200delinsGAGCAGGCCTTGGTGTTGGC	NP_001229381.1:p.Gly394=
NM_001347928.2:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	NP_001334857.1:p.Gly496=
NM_001364314.2:c.1487_1506delinsGAGCAGGCCTTGGTGTTGGC	NP_001351243.1:p.Gly496=
NM_001098627.4:c.1439_1458delinsGAGCAGGCCTTGGTGTTGGC	NP_001092097.2:p.Gly480=
NM_032643.5:c.1439_1458delinsGAGCAGGCCTTGGTGTTGGC	NP_116032.1:p.Gly480=