Canonical Allele Identifier: CA2484364765
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209788436G= , CM000663.2:g.209788436G= GRCh38
NC_000001.10:g.209961781G= , CM000663.1:g.209961781G= GRCh37
NC_000001.9:g.208028404G= NCBI36
NG_007081.2:g.22699C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1388C= ENSP00000512426.1:p.Ala463=
ENST00000696134.1:c.*815C= ENSP00000512427.1:n.*815C=
ENST00000367021.8:c.1388C= MANE Select ENSP00000355988.3:p.Ala463=
ENST00000643798.1:c.*898C= ENSP00000496669.1:n.*898C=
ENST00000367021.7:c.1388C= ENSP00000355988.3:p.Ala463=
ENST00000542854.5:c.1103C= ENSP00000440532.1:p.Ala368=
NM_001206696.1:c.1103C= NP_001193625.1:p.Ala368=
NM_006147.3:c.1388C= NP_006138.1:p.Ala463=
NM_006147.4:c.1388C= MANE Select NP_006138.1:p.Ala463=
NM_001206696.2:c.1103C= NP_001193625.1:p.Ala368=