Canonical Allele Identifier: CA2484369580

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801333G= , CM000663.2:g.209801333G=	GRCh38
NC_000001.10:g.209974678G= , CM000663.1:g.209974678G=	GRCh37
NC_000001.9:g.208041301G=	NCBI36
NG_007081.2:g.9802C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.81C=	ENSP00000512426.1:p.Ile27=
ENST00000696134.1:c.81C=	ENSP00000512427.1:p.Ile27=
ENST00000367021.8:c.81C= MANE Select	ENSP00000355988.3:p.Ile27=
ENST00000643798.1:c.81C=	ENSP00000496669.1:p.Ile27=
ENST00000367021.7:c.81C=	ENSP00000355988.3:p.Ile27=
ENST00000456314.1:c.81C=	ENSP00000403855.1:p.Ile27=
ENST00000542854.5:c.-112+4614C=	ENSP00000440532.1:n.-112+4614C=
NM_001206696.1:c.-112+4614C=	NP_001193625.1:n.-112+4614C=
NM_006147.3:c.81C=	NP_006138.1:p.Ile27=
NM_006147.4:c.81C= MANE Select	NP_006138.1:p.Ile27=
NM_001206696.2:c.-112+4614C=	NP_001193625.1:n.-112+4614C=