Canonical Allele Identifier: CA2484369541
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801214G= , CM000663.2:g.209801214G= GRCh38
NC_000001.10:g.209974559G= , CM000663.1:g.209974559G= GRCh37
NC_000001.9:g.208041182G= NCBI36
NG_007081.2:g.9921C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.174+26C= ENSP00000512426.1:n.174+26C=
ENST00000696134.1:c.174+26C= ENSP00000512427.1:n.174+26C=
ENST00000367021.8:c.174+26C= MANE Select ENSP00000355988.3:n.174+26C=
ENST00000643798.1:c.174+26C= ENSP00000496669.1:n.174+26C=
ENST00000367021.7:c.174+26C= ENSP00000355988.3:n.174+26C=
ENST00000456314.1:c.174+26C= ENSP00000403855.1:n.174+26C=
ENST00000542854.5:c.-111-4662C= ENSP00000440532.1:n.-111-4662C=
NM_001206696.1:c.-111-4662C= NP_001193625.1:n.-111-4662C=
NM_006147.3:c.174+26C= NP_006138.1:n.174+26C=
NM_006147.4:c.174+26C= MANE Select NP_006138.1:n.174+26C=
NM_001206696.2:c.-111-4662C= NP_001193625.1:n.-111-4662C=