Canonical Allele Identifier: CA1742564635
Gene: IRF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128949019_128949021delinsGTC , CM000669.2:g.128949019_128949021delinsGTC GRCh38
NC_000007.13:g.128589073_128589075delinsGTC , CM000669.1:g.128589073_128589075delinsGTC GRCh37
NC_000007.12:g.128376309_128376311delinsGTC NCBI36
NG_012306.1:g.16080_16082delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700148.1:n.1982_1984delinsGTC
ENST00000700151.1:n.4248_4250delinsGTC
ENST00000700152.1:n.3788_3790delinsGTC
ENST00000700153.1:n.3162_3164delinsGTC
ENST00000700154.1:n.1326_1328delinsGTC
ENST00000357234.10:c.*201_*203delinsGTC MANE Select ENSP00000349770.5:n.*201_*203delinsGTC
ENST00000489702.6:c.*201_*203delinsGTC ENSP00000418037.2:n.*201_*203delinsGTC
ENST00000249375.8:c.*201_*203delinsGTC ENSP00000249375.4:n.*201_*203delinsGTC
ENST00000402030.6:c.*201_*203delinsGTC ENSP00000385352.2:n.*201_*203delinsGTC
ENST00000465603.5:c.*1226_*1228delinsGTC ENSP00000418534.1:n.*1226_*1228delinsGTC
ENST00000473745.5:c.*201_*203delinsGTC ENSP00000419149.1:n.*201_*203delinsGTC
NM_001098627.3:c.*201_*203delinsGTC NP_001092097.2:n.*201_*203delinsGTC
NM_001098629.2:c.*201_*203delinsGTC NP_001092099.1:n.*201_*203delinsGTC
NM_001098630.2:c.*201_*203delinsGTC NP_001092100.1:n.*201_*203delinsGTC
NM_001242452.2:c.*201_*203delinsGTC NP_001229381.1:n.*201_*203delinsGTC
NM_032643.4:c.*201_*203delinsGTC NP_116032.1:n.*201_*203delinsGTC
XM_005250317.2:c.*201_*203delinsGTC XP_005250374.1:n.*201_*203delinsGTC
XM_006715974.2:c.*201_*203delinsGTC XP_006716037.1:n.*201_*203delinsGTC
XM_011516158.1:c.*201_*203delinsGTC XP_011514460.1:n.*201_*203delinsGTC
XM_011516159.1:c.*201_*203delinsGTC XP_011514461.1:n.*201_*203delinsGTC
XM_011516160.1:c.*201_*203delinsGTC XP_011514462.1:n.*201_*203delinsGTC
XM_011516161.1:c.*201_*203delinsGTC XP_011514463.1:n.*201_*203delinsGTC
XM_011516162.1:c.*201_*203delinsGTC XP_011514464.1:n.*201_*203delinsGTC
XM_011516163.1:c.*201_*203delinsGTC XP_011514465.1:n.*201_*203delinsGTC
XM_011516164.1:c.*201_*203delinsGTC XP_011514466.1:n.*201_*203delinsGTC
NM_001347928.1:c.*201_*203delinsGTC NP_001334857.1:n.*201_*203delinsGTC
NM_001364314.1:c.*201_*203delinsGTC NP_001351243.1:n.*201_*203delinsGTC
XM_011516158.3:c.*201_*203delinsGTC XP_011514460.1:n.*201_*203delinsGTC
XM_011516159.3:c.*201_*203delinsGTC XP_011514461.1:n.*201_*203delinsGTC
NM_001098629.3:c.*201_*203delinsGTC MANE Select NP_001092099.1:n.*201_*203delinsGTC
NM_001098630.3:c.*201_*203delinsGTC NP_001092100.1:n.*201_*203delinsGTC
NM_001242452.3:c.*201_*203delinsGTC NP_001229381.1:n.*201_*203delinsGTC
NM_001347928.2:c.*201_*203delinsGTC NP_001334857.1:n.*201_*203delinsGTC
NM_001364314.2:c.*201_*203delinsGTC NP_001351243.1:n.*201_*203delinsGTC
NM_001098627.4:c.*201_*203delinsGTC NP_001092097.2:n.*201_*203delinsGTC
NM_032643.5:c.*201_*203delinsGTC NP_116032.1:n.*201_*203delinsGTC