Canonical Allele Identifier: CA378978310

Gene: IRF7

Linked Data

• MyVariant Identifiers: chr11:g.613106A>T (hg19) ; chr11:g.613106A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.613106A>T , CM000673.2:g.613106A>T	GRCh38
NC_000011.9:g.613106A>T , CM000673.1:g.613106A>T	GRCh37
NC_000011.8:g.603106A>T	NCBI36
NG_029106.1:g.7894T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348655.11:c.1162T>A	ENSP00000331803.9:p.Phe388Ile
ENST00000469048.6:c.*528T>A	ENSP00000434607.1:n.*528T>A
ENST00000525445.6:c.1249T>A MANE Select	ENSP00000434009.2:p.Phe417Ile
ENST00000528413.6:c.1199T>A	ENSP00000497888.1:n.1199T>A
ENST00000330243.9:c.1288T>A	ENSP00000329411.5:p.Phe430Ile
ENST00000348655.10:c.1162T>A	ENSP00000331803.9:p.Phe388Ile
ENST00000397566.5:c.1288T>A	ENSP00000380697.1:p.Phe430Ile
ENST00000397570.5:c.1201T>A	ENSP00000380700.2:p.Phe401Ile
ENST00000397574.6:c.1249T>A	ENSP00000380704.2:p.Phe417Ile
ENST00000469048.5:c.*528T>A	ENSP00000434607.1:n.*528T>A
ENST00000525445.5:c.931T>A	ENSP00000434009.1:p.Phe311Ile
ENST00000528413.5:n.364T>A
ENST00000531912.1:n.486T>A
ENST00000532326.5:c.*375T>A	ENSP00000436696.1:n.*375T>A
ENST00000533182.5:c.*613T>A	ENSP00000433903.1:n.*613T>A
NM_001572.3:c.1249T>A	NP_001563.2:p.Phe417Ile
NM_004029.2:c.1162T>A	NP_004020.1:p.Phe388Ile
NM_004031.2:c.1288T>A	NP_004022.2:p.Phe430Ile
XM_005252906.2:c.1288T>A	XP_005252963.1:p.Phe430Ile
XM_005252907.2:c.1285T>A	XP_005252964.1:p.Phe429Ile
XM_005252909.2:c.1201T>A	XP_005252966.1:p.Phe401Ile
XM_011520066.1:c.1246T>A	XP_011518368.1:p.Phe416Ile
NM_001572.4:c.1249T>A	NP_001563.2:p.Phe417Ile
NM_004029.3:c.1162T>A	NP_004020.1:p.Phe388Ile
NM_004031.3:c.1288T>A	NP_004022.2:p.Phe430Ile
XM_005252907.3:c.1285T>A	XP_005252964.1:p.Phe429Ile
XM_005252909.3:c.1201T>A	XP_005252966.1:p.Phe401Ile
XM_011520066.3:c.1246T>A	XP_011518368.1:p.Phe416Ile
XM_017017674.1:c.370T>A	XP_016873163.1:p.Phe124Ile
NM_001572.5:c.1249T>A MANE Select	NP_001563.2:p.Phe417Ile
NM_004029.4:c.1162T>A	NP_004020.1:p.Phe388Ile
NM_004031.4:c.1288T>A	NP_004022.2:p.Phe430Ile