Canonical Allele Identifier: CA1947180774

Gene: IRF7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.613094G= , CM000673.2:g.613094G=	GRCh38
NC_000011.9:g.613094G= , CM000673.1:g.613094G=	GRCh37
NC_000011.8:g.603094G=	NCBI36
NG_029106.1:g.7906C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348655.11:c.1174C=	ENSP00000331803.9:p.Gln392=
ENST00000469048.6:c.*540C=	ENSP00000434607.1:n.*540C=
ENST00000525445.6:c.1261C= MANE Select	ENSP00000434009.2:p.Gln421=
ENST00000528413.6:c.1211C=	ENSP00000497888.1:n.1211C=
ENST00000330243.9:c.1300C=	ENSP00000329411.5:p.Gln434=
ENST00000348655.10:c.1174C=	ENSP00000331803.9:p.Gln392=
ENST00000397566.5:c.1300C=	ENSP00000380697.1:p.Gln434=
ENST00000397570.5:c.1213C=	ENSP00000380700.2:p.Gln405=
ENST00000397574.6:c.1261C=	ENSP00000380704.2:p.Gln421=
ENST00000469048.5:c.*540C=	ENSP00000434607.1:n.*540C=
ENST00000525445.5:c.943C=	ENSP00000434009.1:p.Gln315=
ENST00000528413.5:n.376C=
ENST00000531912.1:n.498C=
ENST00000532326.5:c.*387C=	ENSP00000436696.1:n.*387C=
ENST00000533182.5:c.*625C=	ENSP00000433903.1:n.*625C=
NM_001572.3:c.1261C=	NP_001563.2:p.Gln421=
NM_004029.2:c.1174C=	NP_004020.1:p.Gln392=
NM_004031.2:c.1300C=	NP_004022.2:p.Gln434=
XM_005252906.2:c.1300C=	XP_005252963.1:p.Gln434=
XM_005252907.2:c.1297C=	XP_005252964.1:p.Gln433=
XM_005252909.2:c.1213C=	XP_005252966.1:p.Gln405=
XM_011520066.1:c.1258C=	XP_011518368.1:p.Gln420=
NM_001572.4:c.1261C=	NP_001563.2:p.Gln421=
NM_004029.3:c.1174C=	NP_004020.1:p.Gln392=
NM_004031.3:c.1300C=	NP_004022.2:p.Gln434=
XM_005252907.3:c.1297C=	XP_005252964.1:p.Gln433=
XM_005252909.3:c.1213C=	XP_005252966.1:p.Gln405=
XM_011520066.3:c.1258C=	XP_011518368.1:p.Gln420=
XM_017017674.1:c.382C=	XP_016873163.1:p.Gln128=
NM_001572.5:c.1261C= MANE Select	NP_001563.2:p.Gln421=
NM_004029.4:c.1174C=	NP_004020.1:p.Gln392=
NM_004031.4:c.1300C=	NP_004022.2:p.Gln434=