Canonical Allele Identifier: CA378978452

Gene: IRF7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.613215A>G , CM000673.2:g.613215A>G	GRCh38
NC_000011.9:g.613215A>G , CM000673.1:g.613215A>G	GRCh37
NC_000011.8:g.603215A>G	NCBI36
NG_029106.1:g.7785T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001572.5:c.1228T>C MANE Select	NP_001563.2:p.Phe410Leu
ENST00000525445.6:c.1228T>C MANE Select	ENSP00000434009.2:p.Phe410Leu
NM_001572.3:c.1228T>C	NP_001563.2:p.Phe410Leu
NM_001572.4:c.1228T>C	NP_001563.2:p.Phe410Leu
NM_004029.2:c.1141T>C	NP_004020.1:p.Phe381Leu
NM_004029.3:c.1141T>C	NP_004020.1:p.Phe381Leu
NM_004029.4:c.1141T>C	NP_004020.1:p.Phe381Leu
NM_004031.2:c.1267T>C	NP_004022.2:p.Phe423Leu
NM_004031.3:c.1267T>C	NP_004022.2:p.Phe423Leu
NM_004031.4:c.1267T>C	NP_004022.2:p.Phe423Leu
ENST00000330243.9:c.1267T>C	ENSP00000329411.5:p.Phe423Leu
ENST00000348655.10:c.1141T>C	ENSP00000331803.9:p.Phe381Leu
ENST00000348655.11:c.1141T>C	ENSP00000331803.9:p.Phe381Leu
ENST00000397566.5:c.1267T>C	ENSP00000380697.1:p.Phe423Leu
ENST00000397570.5:c.1180T>C	ENSP00000380700.2:p.Phe394Leu
ENST00000397574.6:c.1228T>C	ENSP00000380704.2:p.Phe410Leu
ENST00000469048.5:c.*507T>C	ENSP00000434607.1:n.*507T>C
ENST00000469048.6:c.*507T>C	ENSP00000434607.1:n.*507T>C
ENST00000525445.5:c.910T>C	ENSP00000434009.1:p.Phe304Leu
ENST00000528413.5:n.338-83T>C
ENST00000528413.6:c.1178T>C	ENSP00000497888.1:n.1178T>C
ENST00000531912.1:n.377T>C
ENST00000532326.5:c.*354T>C	ENSP00000436696.1:n.*354T>C
ENST00000533182.5:c.*592T>C	ENSP00000433903.1:n.*592T>C
XM_005252906.2:c.1267T>C	XP_005252963.1:p.Phe423Leu
XM_005252907.2:c.1264T>C	XP_005252964.1:p.Phe422Leu
XM_005252907.3:c.1264T>C	XP_005252964.1:p.Phe422Leu
XM_005252909.2:c.1180T>C	XP_005252966.1:p.Phe394Leu
XM_005252909.3:c.1180T>C	XP_005252966.1:p.Phe394Leu
XM_011520066.1:c.1225T>C	XP_011518368.1:p.Phe409Leu
XM_011520066.3:c.1225T>C	XP_011518368.1:p.Phe409Leu
XM_017017674.1:c.349T>C	XP_016873163.1:p.Phe117Leu