Canonical Allele Identifier: CA2484365194

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209789589T= , CM000663.2:g.209789589T=	GRCh38
NC_000001.10:g.209962934T= , CM000663.1:g.209962934T=	GRCh37
NC_000001.9:g.208029557T=	NCBI36
NG_007081.2:g.21546A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696133.1:c.1179+78A=	ENSP00000512426.1:n.1179+78A=
ENST00000696134.1:c.*606+78A=	ENSP00000512427.1:n.*606+78A=
ENST00000367021.8:c.1179+78A= MANE Select	ENSP00000355988.3:n.1179+78A=
ENST00000643798.1:c.*689+78A=	ENSP00000496669.1:n.*689+78A=
ENST00000367021.7:c.1179+78A=	ENSP00000355988.3:n.1179+78A=
ENST00000542854.5:c.894+78A=	ENSP00000440532.1:n.894+78A=
NM_001206696.1:c.894+78A=	NP_001193625.1:n.894+78A=
NM_006147.3:c.1179+78A=	NP_006138.1:n.1179+78A=
NM_006147.4:c.1179+78A= MANE Select	NP_006138.1:n.1179+78A=
NM_001206696.2:c.894+78A=	NP_001193625.1:n.894+78A=