Canonical Allele Identifier: CA1377153
Community Standard Title: NM_006147.4(IRF6):c.1259G>A (p.Arg420His)
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209788565C>T , CM000663.2:g.209788565C>T GRCh38
NC_000001.10:g.209961910C>T , CM000663.1:g.209961910C>T GRCh37
NC_000001.9:g.208028533C>T NCBI36
NG_007081.2:g.22570G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006147.4:c.1259G>A MANE Select NP_006138.1:p.Arg420His
ENST00000367021.8:c.1259G>A MANE Select ENSP00000355988.3:p.Arg420His
NM_001206696.1:c.974G>A NP_001193625.1:p.Arg325His
NM_001206696.2:c.974G>A NP_001193625.1:p.Arg325His
NM_006147.3:c.1259G>A NP_006138.1:p.Arg420His
ENST00000367021.7:c.1259G>A ENSP00000355988.3:p.Arg420His
ENST00000542854.5:c.974G>A ENSP00000440532.1:p.Arg325His
ENST00000643798.1:c.*769G>A ENSP00000496669.1:n.*769G>A
ENST00000696133.1:c.1259G>A ENSP00000512426.1:p.Arg420His
ENST00000696134.1:c.*686G>A ENSP00000512427.1:n.*686G>A