Canonical Allele Identifier: CA5783996

Gene: IRF7

Linked Data

• ClinVar Variation Id: 1170389
• ClinVar RCV Id: RCV001522706 ; RCV001655788 ; RCV003487413
• dbSNP Id: rs1061501
• ExAC: 11:614864 C / T
• gnomAD v2: 11-614864-C-T
• gnomAD v3: 11-614864-C-T
• gnomAD v4: 11-614864-C-T
• MyVariant Identifiers: chr11:g.614864C>T (hg19) ; chr11:g.614864C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.614864C>T , CM000673.2:g.614864C>T	GRCh38
NC_000011.9:g.614864C>T , CM000673.1:g.614864C>T	GRCh37
NC_000011.8:g.604864C>T	NCBI36
NG_029106.1:g.6136G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348655.11:c.327G>A	ENSP00000331803.9:p.Arg109=
ENST00000469048.6:c.327G>A	ENSP00000434607.1:p.Arg109=
ENST00000525445.6:c.327G>A MANE Select	ENSP00000434009.2:p.Arg109=
ENST00000528413.6:c.277G>A	ENSP00000497888.1:n.277G>A
ENST00000647801.1:c.366G>A	ENSP00000497421.1:p.Arg122=
ENST00000649187.1:c.327G>A	ENSP00000497234.1:p.Arg109=
ENST00000330243.9:c.366G>A	ENSP00000329411.5:p.Arg122=
ENST00000348655.10:c.327G>A	ENSP00000331803.9:p.Arg109=
ENST00000397566.5:c.366G>A	ENSP00000380697.1:p.Arg122=
ENST00000397570.5:c.366G>A	ENSP00000380700.2:p.Arg122=
ENST00000397574.6:c.327G>A	ENSP00000380704.2:p.Arg109=
ENST00000469048.5:c.327G>A	ENSP00000434607.1:p.Arg109=
ENST00000525445.5:c.9G>A	ENSP00000434009.1:p.Arg3=
ENST00000527160.1:n.24G>A
ENST00000532096.1:n.613G>A
ENST00000532326.5:c.327G>A	ENSP00000436696.1:p.Arg109=
ENST00000532788.1:c.366G>A	ENSP00000432403.1:p.Arg122=
ENST00000533182.5:c.327G>A	ENSP00000433903.1:p.Arg109=
ENST00000533190.1:c.*8G>A	ENSP00000434524.1:n.*8G>A
NM_001572.3:c.327G>A	NP_001563.2:p.Arg109=
NM_004029.2:c.327G>A	NP_004020.1:p.Arg109=
NM_004031.2:c.366G>A	NP_004022.2:p.Arg122=
XM_005252906.2:c.366G>A	XP_005252963.1:p.Arg122=
XM_005252907.2:c.366G>A	XP_005252964.1:p.Arg122=
XM_005252909.2:c.366G>A	XP_005252966.1:p.Arg122=
XM_011520066.1:c.327G>A	XP_011518368.1:p.Arg109=
NM_001572.4:c.327G>A	NP_001563.2:p.Arg109=
NM_004029.3:c.327G>A	NP_004020.1:p.Arg109=
NM_004031.3:c.366G>A	NP_004022.2:p.Arg122=
XM_005252907.3:c.366G>A	XP_005252964.1:p.Arg122=
XM_005252909.3:c.366G>A	XP_005252966.1:p.Arg122=
XM_011520066.3:c.327G>A	XP_011518368.1:p.Arg109=
NM_001572.5:c.327G>A MANE Select	NP_001563.2:p.Arg109=
NM_004029.4:c.327G>A	NP_004020.1:p.Arg109=
NM_004031.4:c.366G>A	NP_004022.2:p.Arg122=