Canonical Allele Identifier: CA2484369535

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801204_209801207delinsATCC , CM000663.2:g.209801204_209801207delinsATCC	GRCh38
NC_000001.10:g.209974549_209974552delinsATCC , CM000663.1:g.209974549_209974552delinsATCC	GRCh37
NC_000001.9:g.208041172_208041175delinsATCC	NCBI36
NG_007081.2:g.9928_9931delinsGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.174+33_174+36delinsGGAT	ENSP00000512426.1:n.174+33_174+36delinsGGAT
ENST00000696134.1:c.174+33_174+36delinsGGAT	ENSP00000512427.1:n.174+33_174+36delinsGGAT
ENST00000367021.8:c.174+33_174+36delinsGGAT MANE Select	ENSP00000355988.3:n.174+33_174+36delinsGGAT
ENST00000643798.1:c.174+33_174+36delinsGGAT	ENSP00000496669.1:n.174+33_174+36delinsGGAT
ENST00000367021.7:c.174+33_174+36delinsGGAT	ENSP00000355988.3:n.174+33_174+36delinsGGAT
ENST00000456314.1:c.174+33_174+36delinsGGAT	ENSP00000403855.1:n.174+33_174+36delinsGGAT
ENST00000542854.5:c.-111-4655_-111-4652delinsGGAT	ENSP00000440532.1:n.-111-4655_-111-4652delinsGGAT
NM_001206696.1:c.-111-4655_-111-4652delinsGGAT	NP_001193625.1:n.-111-4655_-111-4652delinsGGAT
NM_006147.3:c.174+33_174+36delinsGGAT	NP_006138.1:n.174+33_174+36delinsGGAT
NM_006147.4:c.174+33_174+36delinsGGAT MANE Select	NP_006138.1:n.174+33_174+36delinsGGAT
NM_001206696.2:c.-111-4655_-111-4652delinsGGAT	NP_001193625.1:n.-111-4655_-111-4652delinsGGAT