Canonical Allele Identifier: CA1143403007
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801213G= , CM000663.2:g.209801213G= GRCh38
NC_000001.10:g.209974558G= , CM000663.1:g.209974558G= GRCh37
NC_000001.9:g.208041181G= NCBI36
NG_007081.2:g.9922C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.174+27C= ENSP00000512426.1:n.174+27C=
ENST00000696134.1:c.174+27C= ENSP00000512427.1:n.174+27C=
ENST00000367021.8:c.174+27C= MANE Select ENSP00000355988.3:n.174+27C=
ENST00000643798.1:c.174+27C= ENSP00000496669.1:n.174+27C=
ENST00000367021.7:c.174+27C= ENSP00000355988.3:n.174+27C=
ENST00000456314.1:c.174+27C= ENSP00000403855.1:n.174+27C=
ENST00000542854.5:c.-111-4661C= ENSP00000440532.1:n.-111-4661C=
NM_001206696.1:c.-111-4661C= NP_001193625.1:n.-111-4661C=
NM_006147.3:c.174+27C= NP_006138.1:n.174+27C=
NM_006147.4:c.174+27C= MANE Select NP_006138.1:n.174+27C=
NM_001206696.2:c.-111-4661C= NP_001193625.1:n.-111-4661C=