Canonical Allele Identifier: CA833144124

Gene: IRF5

Linked Data

• dbSNP Id: rs1410315128
• gnomAD v3: 7-128948916-G-GTCCT
• gnomAD v4: 7-128948916-G-GTCCT
• MyVariant Identifiers: chr7:g.128588970_128588971insTCCT (hg19) ; chr7:g.128948916_128948917insTCCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128948917_128948920dup , CM000669.2:g.128948917_128948920dup	GRCh38
NC_000007.13:g.128588971_128588974dup , CM000669.1:g.128588971_128588974dup	GRCh37
NC_000007.12:g.128376207_128376210dup	NCBI36
NG_012306.1:g.15978_15981dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700148.1:n.1880_1883dup
ENST00000700151.1:n.4146_4149dup
ENST00000700152.1:n.3686_3689dup
ENST00000700153.1:n.3060_3063dup
ENST00000700154.1:n.1224_1227dup
ENST00000357234.10:c.*99_*102dup MANE Select	ENSP00000349770.5:n.*99_*102dup
ENST00000489702.6:c.*99_*102dup	ENSP00000418037.2:n.*99_*102dup
ENST00000249375.8:c.*99_*102dup	ENSP00000249375.4:n.*99_*102dup
ENST00000402030.6:c.*99_*102dup	ENSP00000385352.2:n.*99_*102dup
ENST00000465603.5:c.*1124_*1127dup	ENSP00000418534.1:n.*1124_*1127dup
ENST00000473745.5:c.*99_*102dup	ENSP00000419149.1:n.*99_*102dup
ENST00000619830.1:c.*1094_*1097dup	ENSP00000483292.1:n.*1094_*1097dup
NM_001098627.3:c.*99_*102dup	NP_001092097.2:n.*99_*102dup
NM_001098629.2:c.*99_*102dup	NP_001092099.1:n.*99_*102dup
NM_001098630.2:c.*99_*102dup	NP_001092100.1:n.*99_*102dup
NM_001242452.2:c.*99_*102dup	NP_001229381.1:n.*99_*102dup
NM_032643.4:c.*99_*102dup	NP_116032.1:n.*99_*102dup
XM_005250317.2:c.*99_*102dup	XP_005250374.1:n.*99_*102dup
XM_006715974.2:c.*99_*102dup	XP_006716037.1:n.*99_*102dup
XM_011516158.1:c.*99_*102dup	XP_011514460.1:n.*99_*102dup
XM_011516159.1:c.*99_*102dup	XP_011514461.1:n.*99_*102dup
XM_011516160.1:c.*99_*102dup	XP_011514462.1:n.*99_*102dup
XM_011516161.1:c.*99_*102dup	XP_011514463.1:n.*99_*102dup
XM_011516162.1:c.*99_*102dup	XP_011514464.1:n.*99_*102dup
XM_011516163.1:c.*99_*102dup	XP_011514465.1:n.*99_*102dup
XM_011516164.1:c.*99_*102dup	XP_011514466.1:n.*99_*102dup
NM_001347928.1:c.*99_*102dup	NP_001334857.1:n.*99_*102dup
NM_001364314.1:c.*99_*102dup	NP_001351243.1:n.*99_*102dup
XM_011516158.3:c.*99_*102dup	XP_011514460.1:n.*99_*102dup
XM_011516159.3:c.*99_*102dup	XP_011514461.1:n.*99_*102dup
NM_001098629.3:c.*99_*102dup MANE Select	NP_001092099.1:n.*99_*102dup
NM_001098630.3:c.*99_*102dup	NP_001092100.1:n.*99_*102dup
NM_001242452.3:c.*99_*102dup	NP_001229381.1:n.*99_*102dup
NM_001347928.2:c.*99_*102dup	NP_001334857.1:n.*99_*102dup
NM_001364314.2:c.*99_*102dup	NP_001351243.1:n.*99_*102dup
NM_001098627.4:c.*99_*102dup	NP_001092097.2:n.*99_*102dup
NM_032643.5:c.*99_*102dup	NP_116032.1:n.*99_*102dup