Canonical Allele Identifier: CA2484366082
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209792257A= , CM000663.2:g.209792257A= GRCh38
NC_000001.10:g.209965602A= , CM000663.1:g.209965602A= GRCh37
NC_000001.9:g.208032225A= NCBI36
NG_007081.2:g.18878T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.667+12T= ENSP00000512426.1:n.667+12T=
ENST00000696134.1:c.667+12T= ENSP00000512427.1:n.667+12T=
ENST00000367021.8:c.667+12T= MANE Select ENSP00000355988.3:n.667+12T=
ENST00000643798.1:c.*177+12T= ENSP00000496669.1:n.*177+12T=
ENST00000367021.7:c.667+12T= ENSP00000355988.3:n.667+12T=
ENST00000456314.1:c.667+12T= ENSP00000403855.1:n.667+12T=
ENST00000464698.1:n.446+12T=
ENST00000542854.5:c.382+12T= ENSP00000440532.1:n.382+12T=
NM_001206696.1:c.382+12T= NP_001193625.1:n.382+12T=
NM_006147.3:c.667+12T= NP_006138.1:n.667+12T=
NM_006147.4:c.667+12T= MANE Select NP_006138.1:n.667+12T=
NM_001206696.2:c.382+12T= NP_001193625.1:n.382+12T=