Canonical Allele Identifier: CA2650334226

Gene: IRF6

Linked Data

• gnomAD v4: 1-209788652-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209788652_209788653insT , CM000663.2:g.209788652_209788653insT	GRCh38
NC_000001.10:g.209961997_209961998insT , CM000663.1:g.209961997_209961998insT	GRCh37
NC_000001.9:g.208028620_208028621insT	NCBI36
NG_007081.2:g.22482_22483insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000696133.1:c.1180-9_1180-8insA	ENSP00000512426.1:n.1180-9_1180-8insA
ENST00000696134.1:c.*607-9_*607-8insA	ENSP00000512427.1:n.*607-9_*607-8insA
ENST00000367021.8:c.1180-9_1180-8insA MANE Select	ENSP00000355988.3:n.1180-9_1180-8insA
ENST00000643798.1:c.*690-9_*690-8insA	ENSP00000496669.1:n.*690-9_*690-8insA
ENST00000367021.7:c.1180-9_1180-8insA	ENSP00000355988.3:n.1180-9_1180-8insA
ENST00000542854.5:c.895-9_895-8insA	ENSP00000440532.1:n.895-9_895-8insA
NM_001206696.1:c.895-9_895-8insA	NP_001193625.1:n.895-9_895-8insA
NM_006147.3:c.1180-9_1180-8insA	NP_006138.1:n.1180-9_1180-8insA
NM_006147.4:c.1180-9_1180-8insA MANE Select	NP_006138.1:n.1180-9_1180-8insA
NM_001206696.2:c.895-9_895-8insA	NP_001193625.1:n.895-9_895-8insA