Canonical Allele Identifier: CA1947181197
Community Standard Title: NM_001572.5(IRF7):c.1228T= (p.Phe410=)
Gene: IRF7 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_001572.5:c.1228T= MANE Select NP_001563.2:p.Phe410=
ENST00000525445.6:c.1228T= MANE Select ENSP00000434009.2:p.Phe410=
NM_001572.3:c.1228T= NP_001563.2:p.Phe410=
NM_001572.4:c.1228T= NP_001563.2:p.Phe410=
NM_004029.2:c.1141T= NP_004020.1:p.Phe381=
NM_004029.3:c.1141T= NP_004020.1:p.Phe381=
NM_004029.4:c.1141T= NP_004020.1:p.Phe381=
NM_004031.2:c.1267T= NP_004022.2:p.Phe423=
NM_004031.3:c.1267T= NP_004022.2:p.Phe423=
NM_004031.4:c.1267T= NP_004022.2:p.Phe423=
ENST00000330243.9:c.1267T= ENSP00000329411.5:p.Phe423=
ENST00000348655.10:c.1141T= ENSP00000331803.9:p.Phe381=
ENST00000348655.11:c.1141T= ENSP00000331803.9:p.Phe381=
ENST00000397566.5:c.1267T= ENSP00000380697.1:p.Phe423=
ENST00000397570.5:c.1180T= ENSP00000380700.2:p.Phe394=
ENST00000397574.6:c.1228T= ENSP00000380704.2:p.Phe410=
ENST00000469048.5:c.*507T= ENSP00000434607.1:n.*507T=
ENST00000469048.6:c.*507T= ENSP00000434607.1:n.*507T=
ENST00000525445.5:c.910T= ENSP00000434009.1:p.Phe304=
ENST00000528413.5:n.338-83T=
ENST00000528413.6:c.1178T= ENSP00000497888.1:n.1178T=
ENST00000531912.1:n.377T=
ENST00000532326.5:c.*354T= ENSP00000436696.1:n.*354T=
ENST00000533182.5:c.*592T= ENSP00000433903.1:n.*592T=
XM_005252906.2:c.1267T= XP_005252963.1:p.Phe423=
XM_005252907.2:c.1264T= XP_005252964.1:p.Phe422=
XM_005252907.3:c.1264T= XP_005252964.1:p.Phe422=
XM_005252909.2:c.1180T= XP_005252966.1:p.Phe394=
XM_005252909.3:c.1180T= XP_005252966.1:p.Phe394=
XM_011520066.1:c.1225T= XP_011518368.1:p.Phe409=
XM_011520066.3:c.1225T= XP_011518368.1:p.Phe409=
XM_017017674.1:c.349T= XP_016873163.1:p.Phe117=