Canonical Allele Identifier: CA1742563757
Gene: IRF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128948739_128948772delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG , CM000669.2:g.128948739_128948772delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG GRCh38
NC_000007.13:g.128588793_128588826delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG , CM000669.1:g.128588793_128588826delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG GRCh37
NC_000007.12:g.128376029_128376062delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NCBI36
NG_012306.1:g.15800_15833delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700148.1:n.1702_1735delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG
ENST00000700151.1:n.3968_4001delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG
ENST00000700152.1:n.3508_3541delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG
ENST00000700153.1:n.2882_2915delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG
ENST00000700154.1:n.1046_1079delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG
ENST00000357234.10:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG MANE Select ENSP00000349770.5:p.Pro489=
ENST00000489702.6:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG ENSP00000418037.2:p.Pro489=
ENST00000249375.8:c.1418_1451delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG ENSP00000249375.4:p.Pro473=
ENST00000357234.9:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG ENSP00000349770.5:p.Pro489=
ENST00000402030.6:c.1418_1451delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG ENSP00000385352.2:p.Pro473=
ENST00000465603.5:c.*946_*979delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG ENSP00000418534.1:n.*946_*979delinsCTGTGGCCCAGGCCCCTCCTGGAGCA...
ENST00000473745.5:c.1418_1451delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG ENSP00000419149.1:p.Pro473=
ENST00000477535.5:c.1160_1193delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG ENSP00000419950.1:p.Pro387=
ENST00000619830.1:c.*916_*949delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG ENSP00000483292.1:n.*916_*949delinsCTGTGGCCCAGGCCCCTCCTGGAGCA...
NM_001098627.3:c.1418_1451delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001092097.2:p.Pro473=
NM_001098629.2:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001092099.1:p.Pro489=
NM_001098630.2:c.1418_1451delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001092100.1:p.Pro473=
NM_001242452.2:c.1160_1193delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001229381.1:p.Pro387=
NM_032643.4:c.1418_1451delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_116032.1:p.Pro473=
XM_005250317.2:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_005250374.1:p.Pro489=
XM_006715974.2:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_006716037.1:p.Pro489=
XM_011516158.1:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_011514460.1:p.Pro489=
XM_011516159.1:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_011514461.1:p.Pro489=
XM_011516160.1:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_011514462.1:p.Pro489=
XM_011516161.1:c.1436_1469delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_011514463.1:p.Pro479=
XM_011516162.1:c.1388_1421delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_011514464.1:p.Pro463=
XM_011516163.1:c.1388_1421delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_011514465.1:p.Pro463=
XM_011516164.1:c.1388_1421delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_011514466.1:p.Pro463=
NM_001347928.1:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001334857.1:p.Pro489=
NM_001364314.1:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001351243.1:p.Pro489=
XM_011516158.3:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_011514460.1:p.Pro489=
XM_011516159.3:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG XP_011514461.1:p.Pro489=
NM_001098629.3:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG MANE Select NP_001092099.1:p.Pro489=
NM_001098630.3:c.1418_1451delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001092100.1:p.Pro473=
NM_001242452.3:c.1160_1193delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001229381.1:p.Pro387=
NM_001347928.2:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001334857.1:p.Pro489=
NM_001364314.2:c.1466_1499delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001351243.1:p.Pro489=
NM_001098627.4:c.1418_1451delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_001092097.2:p.Pro473=
NM_032643.5:c.1418_1451delinsCTGTGGCCCAGGCCCCTCCTGGAGCAGGCCTTGG NP_116032.1:p.Pro473=