Canonical Allele Identifier: CA1144229119

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801349A= , CM000663.2:g.209801349A=	GRCh38
NC_000001.10:g.209974694A= , CM000663.1:g.209974694A=	GRCh37
NC_000001.9:g.208041317A=	NCBI36
NG_007081.2:g.9786T=

Transcript Alleles

HGVS	Amino-acid Change
NM_006147.4:c.65T= MANE Select	NP_006138.1:p.Leu22=
ENST00000367021.8:c.65T= MANE Select	ENSP00000355988.3:p.Leu22=
NM_001206696.1:c.-112+4598T=	NP_001193625.1:n.-112+4598T=
NM_001206696.2:c.-112+4598T=	NP_001193625.1:n.-112+4598T=
NM_006147.3:c.65T=	NP_006138.1:p.Leu22=
ENST00000367021.7:c.65T=	ENSP00000355988.3:p.Leu22=
ENST00000456314.1:c.65T=	ENSP00000403855.1:p.Leu22=
ENST00000542854.5:c.-112+4598T=	ENSP00000440532.1:n.-112+4598T=
ENST00000643798.1:c.65T=	ENSP00000496669.1:p.Leu22=
ENST00000696133.1:c.65T=	ENSP00000512426.1:p.Leu22=
ENST00000696134.1:c.65T=	ENSP00000512427.1:p.Leu22=