Canonical Allele Identifier: CA423026503

Gene: IRF6

Linked Data

• MyVariant Identifiers: chr1:g.209961948A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209788603A>T , CM000663.2:g.209788603A>T	GRCh38
NC_000001.10:g.209961948A>T , CM000663.1:g.209961948A>T	GRCh37
NC_000001.9:g.208028571A>T	NCBI36
NG_007081.2:g.22532T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696133.1:c.1221T>A	ENSP00000512426.1:p.Ser407=
ENST00000696134.1:c.*648T>A	ENSP00000512427.1:n.*648T>A
ENST00000367021.8:c.1221T>A MANE Select	ENSP00000355988.3:p.Ser407=
ENST00000643798.1:c.*731T>A	ENSP00000496669.1:n.*731T>A
ENST00000367021.7:c.1221T>A	ENSP00000355988.3:p.Ser407=
ENST00000542854.5:c.936T>A	ENSP00000440532.1:p.Ser312=
NM_001206696.1:c.936T>A	NP_001193625.1:p.Ser312=
NM_006147.3:c.1221T>A	NP_006138.1:p.Ser407=
NM_006147.4:c.1221T>A MANE Select	NP_006138.1:p.Ser407=
NM_001206696.2:c.936T>A	NP_001193625.1:p.Ser312=