Canonical Allele Identifier: CA1011779914

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801184_209801185insGA , CM000663.2:g.209801184_209801185insGA	GRCh38
NC_000001.10:g.209974529_209974530insGA , CM000663.1:g.209974529_209974530insGA	GRCh37
NC_000001.9:g.208041152_208041153insGA	NCBI36
NG_007081.2:g.9951_9952insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.174+56_174+57insCT	ENSP00000512426.1:n.174+56_174+57insCT
ENST00000696134.1:c.174+56_174+57insCT	ENSP00000512427.1:n.174+56_174+57insCT
ENST00000367021.8:c.174+56_174+57insCT MANE Select	ENSP00000355988.3:n.174+56_174+57insCT
ENST00000643798.1:c.174+56_174+57insCT	ENSP00000496669.1:n.174+56_174+57insCT
ENST00000367021.7:c.174+56_174+57insCT	ENSP00000355988.3:n.174+56_174+57insCT
ENST00000456314.1:c.174+56_174+57insCT	ENSP00000403855.1:n.174+56_174+57insCT
ENST00000542854.5:c.-111-4632_-111-4631insCT	ENSP00000440532.1:n.-111-4632_-111-4631insCT
NM_001206696.1:c.-111-4632_-111-4631insCT	NP_001193625.1:n.-111-4632_-111-4631insCT
NM_006147.3:c.174+56_174+57insCT	NP_006138.1:n.174+56_174+57insCT
NM_006147.4:c.174+56_174+57insCT MANE Select	NP_006138.1:n.174+56_174+57insCT
NM_001206696.2:c.-111-4632_-111-4631insCT	NP_001193625.1:n.-111-4632_-111-4631insCT