Canonical Allele Identifier: CA378977205

Gene: IRF7

Linked Data

• MyVariant Identifiers: chr11:g.613096C>A (hg19) ; chr11:g.613096C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.613096C>A , CM000673.2:g.613096C>A	GRCh38
NC_000011.9:g.613096C>A , CM000673.1:g.613096C>A	GRCh37
NC_000011.8:g.603096C>A	NCBI36
NG_029106.1:g.7904G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348655.11:c.1172G>T	ENSP00000331803.9:p.Arg391Leu
ENST00000469048.6:c.*538G>T	ENSP00000434607.1:n.*538G>T
ENST00000525445.6:c.1259G>T MANE Select	ENSP00000434009.2:p.Arg420Leu
ENST00000528413.6:c.1209G>T	ENSP00000497888.1:n.1209G>T
ENST00000330243.9:c.1298G>T	ENSP00000329411.5:p.Arg433Leu
ENST00000348655.10:c.1172G>T	ENSP00000331803.9:p.Arg391Leu
ENST00000397566.5:c.1298G>T	ENSP00000380697.1:p.Arg433Leu
ENST00000397570.5:c.1211G>T	ENSP00000380700.2:p.Arg404Leu
ENST00000397574.6:c.1259G>T	ENSP00000380704.2:p.Arg420Leu
ENST00000469048.5:c.*538G>T	ENSP00000434607.1:n.*538G>T
ENST00000525445.5:c.941G>T	ENSP00000434009.1:p.Arg314Leu
ENST00000528413.5:n.374G>T
ENST00000531912.1:n.496G>T
ENST00000532326.5:c.*385G>T	ENSP00000436696.1:n.*385G>T
ENST00000533182.5:c.*623G>T	ENSP00000433903.1:n.*623G>T
NM_001572.3:c.1259G>T	NP_001563.2:p.Arg420Leu
NM_004029.2:c.1172G>T	NP_004020.1:p.Arg391Leu
NM_004031.2:c.1298G>T	NP_004022.2:p.Arg433Leu
XM_005252906.2:c.1298G>T	XP_005252963.1:p.Arg433Leu
XM_005252907.2:c.1295G>T	XP_005252964.1:p.Arg432Leu
XM_005252909.2:c.1211G>T	XP_005252966.1:p.Arg404Leu
XM_011520066.1:c.1256G>T	XP_011518368.1:p.Arg419Leu
NM_001572.4:c.1259G>T	NP_001563.2:p.Arg420Leu
NM_004029.3:c.1172G>T	NP_004020.1:p.Arg391Leu
NM_004031.3:c.1298G>T	NP_004022.2:p.Arg433Leu
XM_005252907.3:c.1295G>T	XP_005252964.1:p.Arg432Leu
XM_005252909.3:c.1211G>T	XP_005252966.1:p.Arg404Leu
XM_011520066.3:c.1256G>T	XP_011518368.1:p.Arg419Leu
XM_017017674.1:c.380G>T	XP_016873163.1:p.Arg127Leu
NM_001572.5:c.1259G>T MANE Select	NP_001563.2:p.Arg420Leu
NM_004029.4:c.1172G>T	NP_004020.1:p.Arg391Leu
NM_004031.4:c.1298G>T	NP_004022.2:p.Arg433Leu