Canonical Allele Identifier: CA2650336334

Gene: IRF6

Linked Data

• gnomAD v4: 1-209801388-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801390del , CM000663.2:g.209801390del	GRCh38
NC_000001.10:g.209974735del , CM000663.1:g.209974735del	GRCh37
NC_000001.9:g.208041358del	NCBI36
NG_007081.2:g.9746del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.25del	ENSP00000512426.1:p.Arg9GlyfsTer2
ENST00000696134.1:c.25del	ENSP00000512427.1:p.Arg9GlyfsTer2
ENST00000367021.8:c.25del MANE Select	ENSP00000355988.3:p.Arg9GlyfsTer2
ENST00000643798.1:c.25del	ENSP00000496669.1:p.Arg9GlyfsTer2
ENST00000367021.7:c.25del	ENSP00000355988.3:p.Arg9GlyfsTer2
ENST00000456314.1:c.25del	ENSP00000403855.1:p.Arg9GlyfsTer2
ENST00000542854.5:c.-112+4558del	ENSP00000440532.1:n.-112+4558del
NM_001206696.1:c.-112+4558del	NP_001193625.1:n.-112+4558del
NM_006147.3:c.25del	NP_006138.1:p.Arg9GlyfsTer2
NM_006147.4:c.25del MANE Select	NP_006138.1:p.Arg9GlyfsTer2
NM_001206696.2:c.-112+4558del	NP_001193625.1:n.-112+4558del