Canonical Allele Identifier: CA1947180833
Gene: IRF7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.613104G= , CM000673.2:g.613104G= GRCh38
NC_000011.9:g.613104G= , CM000673.1:g.613104G= GRCh37
NC_000011.8:g.603104G= NCBI36
NG_029106.1:g.7896C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348655.11:c.1164C= ENSP00000331803.9:p.Phe388=
ENST00000469048.6:c.*530C= ENSP00000434607.1:n.*530C=
ENST00000525445.6:c.1251C= MANE Select ENSP00000434009.2:p.Phe417=
ENST00000528413.6:c.1201C= ENSP00000497888.1:n.1201C=
ENST00000330243.9:c.1290C= ENSP00000329411.5:p.Phe430=
ENST00000348655.10:c.1164C= ENSP00000331803.9:p.Phe388=
ENST00000397566.5:c.1290C= ENSP00000380697.1:p.Phe430=
ENST00000397570.5:c.1203C= ENSP00000380700.2:p.Phe401=
ENST00000397574.6:c.1251C= ENSP00000380704.2:p.Phe417=
ENST00000469048.5:c.*530C= ENSP00000434607.1:n.*530C=
ENST00000525445.5:c.933C= ENSP00000434009.1:p.Phe311=
ENST00000528413.5:n.366C=
ENST00000531912.1:n.488C=
ENST00000532326.5:c.*377C= ENSP00000436696.1:n.*377C=
ENST00000533182.5:c.*615C= ENSP00000433903.1:n.*615C=
NM_001572.3:c.1251C= NP_001563.2:p.Phe417=
NM_004029.2:c.1164C= NP_004020.1:p.Phe388=
NM_004031.2:c.1290C= NP_004022.2:p.Phe430=
XM_005252906.2:c.1290C= XP_005252963.1:p.Phe430=
XM_005252907.2:c.1287C= XP_005252964.1:p.Phe429=
XM_005252909.2:c.1203C= XP_005252966.1:p.Phe401=
XM_011520066.1:c.1248C= XP_011518368.1:p.Phe416=
NM_001572.4:c.1251C= NP_001563.2:p.Phe417=
NM_004029.3:c.1164C= NP_004020.1:p.Phe388=
NM_004031.3:c.1290C= NP_004022.2:p.Phe430=
XM_005252907.3:c.1287C= XP_005252964.1:p.Phe429=
XM_005252909.3:c.1203C= XP_005252966.1:p.Phe401=
XM_011520066.3:c.1248C= XP_011518368.1:p.Phe416=
XM_017017674.1:c.372C= XP_016873163.1:p.Phe124=
NM_001572.5:c.1251C= MANE Select NP_001563.2:p.Phe417=
NM_004029.4:c.1164C= NP_004020.1:p.Phe388=
NM_004031.4:c.1290C= NP_004022.2:p.Phe430=