Canonical Allele Identifier: CA1947204133
Community Standard Title: NM_001572.5(IRF7):c.535A= (p.Lys179=)
Gene: IRF7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.614318T= , CM000673.2:g.614318T= GRCh38
NC_000011.9:g.614318T= , CM000673.1:g.614318T= GRCh37
NC_000011.8:g.604318T= NCBI36
NG_029106.1:g.6682A=

Transcript Alleles

HGVS Amino-acid Change
NM_001572.5:c.535A= MANE Select NP_001563.2:p.Lys179=
ENST00000525445.6:c.535A= MANE Select ENSP00000434009.2:p.Lys179=
NM_001572.3:c.535A= NP_001563.2:p.Lys179=
NM_001572.4:c.535A= NP_001563.2:p.Lys179=
NM_004029.2:c.535A= NP_004020.1:p.Lys179=
NM_004029.3:c.535A= NP_004020.1:p.Lys179=
NM_004029.4:c.535A= NP_004020.1:p.Lys179=
NM_004031.2:c.574A= NP_004022.2:p.Lys192=
NM_004031.3:c.574A= NP_004022.2:p.Lys192=
NM_004031.4:c.574A= NP_004022.2:p.Lys192=
ENST00000330243.9:c.574A= ENSP00000329411.5:p.Lys192=
ENST00000348655.10:c.535A= ENSP00000331803.9:p.Lys179=
ENST00000348655.11:c.535A= ENSP00000331803.9:p.Lys179=
ENST00000397566.5:c.574A= ENSP00000380697.1:p.Lys192=
ENST00000397570.5:c.574A= ENSP00000380700.2:p.Lys192=
ENST00000397574.6:c.535A= ENSP00000380704.2:p.Lys179=
ENST00000469048.5:c.453+158A= ENSP00000434607.1:n.453+158A=
ENST00000469048.6:c.453+158A= ENSP00000434607.1:n.453+158A=
ENST00000525445.5:c.217A= ENSP00000434009.1:p.Lys73=
ENST00000525750.1:n.80A=
ENST00000527160.1:n.308A=
ENST00000528413.6:c.485A= ENSP00000497888.1:n.485A=
ENST00000532096.1:n.821A=
ENST00000532326.5:c.450+158A= ENSP00000436696.1:n.450+158A=
ENST00000532788.1:c.492+158A= ENSP00000432403.1:n.492+158A=
ENST00000533182.5:c.453+158A= ENSP00000433903.1:n.453+158A=
XM_005252906.2:c.574A= XP_005252963.1:p.Lys192=
XM_005252907.2:c.571A= XP_005252964.1:p.Lys191=
XM_005252907.3:c.571A= XP_005252964.1:p.Lys191=
XM_005252909.2:c.574A= XP_005252966.1:p.Lys192=
XM_005252909.3:c.574A= XP_005252966.1:p.Lys192=
XM_011520066.1:c.532A= XP_011518368.1:p.Lys178=
XM_011520066.3:c.532A= XP_011518368.1:p.Lys178=
XM_017017674.1:c.-114+158A= XP_016873163.1:n.-114+158A=