Canonical Allele Identifier: CA2484363920
Gene: IRF6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209786003A= , CM000663.2:g.209786003A= GRCh38
NC_000001.10:g.209959348A= , CM000663.1:g.209959348A= GRCh37
NC_000001.9:g.208025971A= NCBI36
NG_007081.2:g.25132T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1401-2294T= ENSP00000512426.1:n.1401-2294T=
ENST00000696134.1:c.*3248T= ENSP00000512427.1:n.*3248T=
ENST00000367021.8:c.*2417T= MANE Select ENSP00000355988.3:n.*2417T=
ENST00000367021.7:c.*2417T= ENSP00000355988.3:n.*2417T=
ENST00000542854.5:c.*2417T= ENSP00000440532.1:n.*2417T=
NM_001206696.1:c.*2417T= NP_001193625.1:n.*2417T=
NM_006147.3:c.*2417T= NP_006138.1:n.*2417T=
NM_006147.4:c.*2417T= MANE Select NP_006138.1:n.*2417T=
NM_001206696.2:c.*2417T= NP_001193625.1:n.*2417T=
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