Canonical Allele Identifier: CA378978299
Gene: IRF7 HGNC NCBI

Linked Data

dbSNP Id: rs1856537812

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000348655.11:c.1164C>A ENSP00000331803.9:p.Phe388Leu
ENST00000469048.6:c.*530C>A ENSP00000434607.1:n.*530C>A
ENST00000525445.6:c.1251C>A MANE Select ENSP00000434009.2:p.Phe417Leu
ENST00000528413.6:c.1201C>A ENSP00000497888.1:n.1201C>A
ENST00000330243.9:c.1290C>A ENSP00000329411.5:p.Phe430Leu
ENST00000348655.10:c.1164C>A ENSP00000331803.9:p.Phe388Leu
ENST00000397566.5:c.1290C>A ENSP00000380697.1:p.Phe430Leu
ENST00000397570.5:c.1203C>A ENSP00000380700.2:p.Phe401Leu
ENST00000397574.6:c.1251C>A ENSP00000380704.2:p.Phe417Leu
ENST00000469048.5:c.*530C>A ENSP00000434607.1:n.*530C>A
ENST00000525445.5:c.933C>A ENSP00000434009.1:p.Phe311Leu
ENST00000528413.5:n.366C>A
ENST00000531912.1:n.488C>A
ENST00000532326.5:c.*377C>A ENSP00000436696.1:n.*377C>A
ENST00000533182.5:c.*615C>A ENSP00000433903.1:n.*615C>A
NM_001572.3:c.1251C>A NP_001563.2:p.Phe417Leu
NM_004029.2:c.1164C>A NP_004020.1:p.Phe388Leu
NM_004031.2:c.1290C>A NP_004022.2:p.Phe430Leu
XM_005252906.2:c.1290C>A XP_005252963.1:p.Phe430Leu
XM_005252907.2:c.1287C>A XP_005252964.1:p.Phe429Leu
XM_005252909.2:c.1203C>A XP_005252966.1:p.Phe401Leu
XM_011520066.1:c.1248C>A XP_011518368.1:p.Phe416Leu
NM_001572.4:c.1251C>A NP_001563.2:p.Phe417Leu
NM_004029.3:c.1164C>A NP_004020.1:p.Phe388Leu
NM_004031.3:c.1290C>A NP_004022.2:p.Phe430Leu
XM_005252907.3:c.1287C>A XP_005252964.1:p.Phe429Leu
XM_005252909.3:c.1203C>A XP_005252966.1:p.Phe401Leu
XM_011520066.3:c.1248C>A XP_011518368.1:p.Phe416Leu
XM_017017674.1:c.372C>A XP_016873163.1:p.Phe124Leu
NM_001572.5:c.1251C>A MANE Select NP_001563.2:p.Phe417Leu
NM_004029.4:c.1164C>A NP_004020.1:p.Phe388Leu
NM_004031.4:c.1290C>A NP_004022.2:p.Phe430Leu