Canonical Allele Identifier: CA1947181180
Community Standard Title: NM_001572.5(IRF7):c.1235A= (p.Gln412=)
Gene: IRF7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.613208T= , CM000673.2:g.613208T= GRCh38
NC_000011.9:g.613208T= , CM000673.1:g.613208T= GRCh37
NC_000011.8:g.603208T= NCBI36
NG_029106.1:g.7792A=

Transcript Alleles

HGVS Amino-acid Change
NM_001572.5:c.1235A= MANE Select NP_001563.2:p.Gln412=
ENST00000525445.6:c.1235A= MANE Select ENSP00000434009.2:p.Gln412=
NM_001572.3:c.1235A= NP_001563.2:p.Gln412=
NM_001572.4:c.1235A= NP_001563.2:p.Gln412=
NM_004029.2:c.1148A= NP_004020.1:p.Gln383=
NM_004029.3:c.1148A= NP_004020.1:p.Gln383=
NM_004029.4:c.1148A= NP_004020.1:p.Gln383=
NM_004031.2:c.1274A= NP_004022.2:p.Gln425=
NM_004031.3:c.1274A= NP_004022.2:p.Gln425=
NM_004031.4:c.1274A= NP_004022.2:p.Gln425=
ENST00000330243.9:c.1274A= ENSP00000329411.5:p.Gln425=
ENST00000348655.10:c.1148A= ENSP00000331803.9:p.Gln383=
ENST00000348655.11:c.1148A= ENSP00000331803.9:p.Gln383=
ENST00000397566.5:c.1274A= ENSP00000380697.1:p.Gln425=
ENST00000397570.5:c.1187A= ENSP00000380700.2:p.Gln396=
ENST00000397574.6:c.1235A= ENSP00000380704.2:p.Gln412=
ENST00000469048.5:c.*514A= ENSP00000434607.1:n.*514A=
ENST00000469048.6:c.*514A= ENSP00000434607.1:n.*514A=
ENST00000525445.5:c.917A= ENSP00000434009.1:p.Gln306=
ENST00000528413.5:n.338-76A=
ENST00000528413.6:c.1185A= ENSP00000497888.1:n.1185A=
ENST00000531912.1:n.384A=
ENST00000532326.5:c.*361A= ENSP00000436696.1:n.*361A=
ENST00000533182.5:c.*599A= ENSP00000433903.1:n.*599A=
XM_005252906.2:c.1274A= XP_005252963.1:p.Gln425=
XM_005252907.2:c.1271A= XP_005252964.1:p.Gln424=
XM_005252907.3:c.1271A= XP_005252964.1:p.Gln424=
XM_005252909.2:c.1187A= XP_005252966.1:p.Gln396=
XM_005252909.3:c.1187A= XP_005252966.1:p.Gln396=
XM_011520066.1:c.1232A= XP_011518368.1:p.Gln411=
XM_011520066.3:c.1232A= XP_011518368.1:p.Gln411=
XM_017017674.1:c.356A= XP_016873163.1:p.Gln119=