Canonical Allele Identifier: CA2484366075

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209792248G= , CM000663.2:g.209792248G=	GRCh38
NC_000001.10:g.209965593G= , CM000663.1:g.209965593G=	GRCh37
NC_000001.9:g.208032216G=	NCBI36
NG_007081.2:g.18887C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.667+21C=	ENSP00000512426.1:n.667+21C=
ENST00000696134.1:c.667+21C=	ENSP00000512427.1:n.667+21C=
ENST00000367021.8:c.667+21C= MANE Select	ENSP00000355988.3:n.667+21C=
ENST00000643798.1:c.*177+21C=	ENSP00000496669.1:n.*177+21C=
ENST00000367021.7:c.667+21C=	ENSP00000355988.3:n.667+21C=
ENST00000456314.1:c.667+21C=	ENSP00000403855.1:n.667+21C=
ENST00000464698.1:n.446+21C=
ENST00000542854.5:c.382+21C=	ENSP00000440532.1:n.382+21C=
NM_001206696.1:c.382+21C=	NP_001193625.1:n.382+21C=
NM_006147.3:c.667+21C=	NP_006138.1:n.667+21C=
NM_006147.4:c.667+21C= MANE Select	NP_006138.1:n.667+21C=
NM_001206696.2:c.382+21C=	NP_001193625.1:n.382+21C=