Canonical Allele Identifier: CA423026941
Gene: IRF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.209961987G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209788642G>A , CM000663.2:g.209788642G>A GRCh38
NC_000001.10:g.209961987G>A , CM000663.1:g.209961987G>A GRCh37
NC_000001.9:g.208028610G>A NCBI36
NG_007081.2:g.22493C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1182C>T ENSP00000512426.1:p.Val394=
ENST00000696134.1:c.*609C>T ENSP00000512427.1:n.*609C>T
ENST00000367021.8:c.1182C>T MANE Select ENSP00000355988.3:p.Val394=
ENST00000643798.1:c.*692C>T ENSP00000496669.1:n.*692C>T
ENST00000367021.7:c.1182C>T ENSP00000355988.3:p.Val394=
ENST00000542854.5:c.897C>T ENSP00000440532.1:p.Val299=
NM_001206696.1:c.897C>T NP_001193625.1:p.Val299=
NM_006147.3:c.1182C>T NP_006138.1:p.Val394=
NM_006147.4:c.1182C>T MANE Select NP_006138.1:p.Val394=
NM_001206696.2:c.897C>T NP_001193625.1:p.Val299=