Canonical Allele Identifier: CA1947180785

Gene: IRF7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.613095C= , CM000673.2:g.613095C=	GRCh38
NC_000011.9:g.613095C= , CM000673.1:g.613095C=	GRCh37
NC_000011.8:g.603095C=	NCBI36
NG_029106.1:g.7905G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348655.11:c.1173G=	ENSP00000331803.9:p.Arg391=
ENST00000469048.6:c.*539G=	ENSP00000434607.1:n.*539G=
ENST00000525445.6:c.1260G= MANE Select	ENSP00000434009.2:p.Arg420=
ENST00000528413.6:c.1210G=	ENSP00000497888.1:n.1210G=
ENST00000330243.9:c.1299G=	ENSP00000329411.5:p.Arg433=
ENST00000348655.10:c.1173G=	ENSP00000331803.9:p.Arg391=
ENST00000397566.5:c.1299G=	ENSP00000380697.1:p.Arg433=
ENST00000397570.5:c.1212G=	ENSP00000380700.2:p.Arg404=
ENST00000397574.6:c.1260G=	ENSP00000380704.2:p.Arg420=
ENST00000469048.5:c.*539G=	ENSP00000434607.1:n.*539G=
ENST00000525445.5:c.942G=	ENSP00000434009.1:p.Arg314=
ENST00000528413.5:n.375G=
ENST00000531912.1:n.497G=
ENST00000532326.5:c.*386G=	ENSP00000436696.1:n.*386G=
ENST00000533182.5:c.*624G=	ENSP00000433903.1:n.*624G=
NM_001572.3:c.1260G=	NP_001563.2:p.Arg420=
NM_004029.2:c.1173G=	NP_004020.1:p.Arg391=
NM_004031.2:c.1299G=	NP_004022.2:p.Arg433=
XM_005252906.2:c.1299G=	XP_005252963.1:p.Arg433=
XM_005252907.2:c.1296G=	XP_005252964.1:p.Arg432=
XM_005252909.2:c.1212G=	XP_005252966.1:p.Arg404=
XM_011520066.1:c.1257G=	XP_011518368.1:p.Arg419=
NM_001572.4:c.1260G=	NP_001563.2:p.Arg420=
NM_004029.3:c.1173G=	NP_004020.1:p.Arg391=
NM_004031.3:c.1299G=	NP_004022.2:p.Arg433=
XM_005252907.3:c.1296G=	XP_005252964.1:p.Arg432=
XM_005252909.3:c.1212G=	XP_005252966.1:p.Arg404=
XM_011520066.3:c.1257G=	XP_011518368.1:p.Arg419=
XM_017017674.1:c.381G=	XP_016873163.1:p.Arg127=
NM_001572.5:c.1260G= MANE Select	NP_001563.2:p.Arg420=
NM_004029.4:c.1173G=	NP_004020.1:p.Arg391=
NM_004031.4:c.1299G=	NP_004022.2:p.Arg433=