Canonical Allele Identifier: CA2484364836
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209788644C= , CM000663.2:g.209788644C= GRCh38
NC_000001.10:g.209961989C= , CM000663.1:g.209961989C= GRCh37
NC_000001.9:g.208028612C= NCBI36
NG_007081.2:g.22491G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1180G= ENSP00000512426.1:p.Val394=
ENST00000696134.1:c.*607G= ENSP00000512427.1:n.*607G=
ENST00000367021.8:c.1180G= MANE Select ENSP00000355988.3:p.Val394=
ENST00000643798.1:c.*690G= ENSP00000496669.1:n.*690G=
ENST00000367021.7:c.1180G= ENSP00000355988.3:p.Val394=
ENST00000542854.5:c.895G= ENSP00000440532.1:p.Val299=
NM_001206696.1:c.895G= NP_001193625.1:p.Val299=
NM_006147.3:c.1180G= NP_006138.1:p.Val394=
NM_006147.4:c.1180G= MANE Select NP_006138.1:p.Val394=
NM_001206696.2:c.895G= NP_001193625.1:p.Val299=