Canonical Allele Identifier: CA2484369561
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801280_209801281delinsCG , CM000663.2:g.209801280_209801281delinsCG GRCh38
NC_000001.10:g.209974625_209974626delinsCG , CM000663.1:g.209974625_209974626delinsCG GRCh37
NC_000001.9:g.208041248_208041249delinsCG NCBI36
NG_007081.2:g.9854_9855delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.133_134delinsCG ENSP00000512426.1:p.Arg45=
ENST00000696134.1:c.133_134delinsCG ENSP00000512427.1:p.Arg45=
ENST00000367021.8:c.133_134delinsCG MANE Select ENSP00000355988.3:p.Arg45=
ENST00000643798.1:c.133_134delinsCG ENSP00000496669.1:p.Arg45=
ENST00000367021.7:c.133_134delinsCG ENSP00000355988.3:p.Arg45=
ENST00000456314.1:c.133_134delinsCG ENSP00000403855.1:p.Arg45=
ENST00000542854.5:c.-112+4666_-112+4667delinsCG ENSP00000440532.1:n.-112+4666_-112+4667delinsCG
NM_001206696.1:c.-112+4666_-112+4667delinsCG NP_001193625.1:n.-112+4666_-112+4667delinsCG
NM_006147.3:c.133_134delinsCG NP_006138.1:p.Arg45=
NM_006147.4:c.133_134delinsCG MANE Select NP_006138.1:p.Arg45=
NM_001206696.2:c.-112+4666_-112+4667delinsCG NP_001193625.1:n.-112+4666_-112+4667delinsCG