Canonical Allele Identifier: CA1146689388
Gene: IRF6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209785771A= , CM000663.2:g.209785771A= GRCh38
NC_000001.10:g.209959116A= , CM000663.1:g.209959116A= GRCh37
NC_000001.9:g.208025739A= NCBI36
NG_007081.2:g.25364T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1401-2062T= ENSP00000512426.1:n.1401-2062T=
ENST00000696134.1:c.*3480T= ENSP00000512427.1:n.*3480T=
ENST00000367021.8:c.*2649T= MANE Select ENSP00000355988.3:n.*2649T=
ENST00000367021.7:c.*2649T= ENSP00000355988.3:n.*2649T=
ENST00000542854.5:c.*2649T= ENSP00000440532.1:n.*2649T=
NM_001206696.1:c.*2649T= NP_001193625.1:n.*2649T=
NM_006147.3:c.*2649T= NP_006138.1:n.*2649T=
NM_006147.4:c.*2649T= MANE Select NP_006138.1:n.*2649T=
NM_001206696.2:c.*2649T= NP_001193625.1:n.*2649T=
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