Canonical Allele Identifier: CA423024687

Gene: IRF6

Linked Data

• MyVariant Identifiers: chr1:g.209961792T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209788447T>C , CM000663.2:g.209788447T>C	GRCh38
NC_000001.10:g.209961792T>C , CM000663.1:g.209961792T>C	GRCh37
NC_000001.9:g.208028415T>C	NCBI36
NG_007081.2:g.22688A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.1377A>G	ENSP00000512426.1:p.Gln459=
ENST00000696134.1:c.*804A>G	ENSP00000512427.1:n.*804A>G
ENST00000367021.8:c.1377A>G MANE Select	ENSP00000355988.3:p.Gln459=
ENST00000643798.1:c.*887A>G	ENSP00000496669.1:n.*887A>G
ENST00000367021.7:c.1377A>G	ENSP00000355988.3:p.Gln459=
ENST00000542854.5:c.1092A>G	ENSP00000440532.1:p.Gln364=
NM_001206696.1:c.1092A>G	NP_001193625.1:p.Gln364=
NM_006147.3:c.1377A>G	NP_006138.1:p.Gln459=
NM_006147.4:c.1377A>G MANE Select	NP_006138.1:p.Gln459=
NM_001206696.2:c.1092A>G	NP_001193625.1:p.Gln364=