Canonical Allele Identifier: CA344575548
Community Standard Title: NM_006147.4(IRF6):c.961G>A (p.Val321Met)
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209790594C>T , CM000663.2:g.209790594C>T GRCh38
NC_000001.10:g.209963939C>T , CM000663.1:g.209963939C>T GRCh37
NC_000001.9:g.208030562C>T NCBI36
NG_007081.2:g.20541G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006147.4:c.961G>A MANE Select NP_006138.1:p.Val321Met
ENST00000367021.8:c.961G>A MANE Select ENSP00000355988.3:p.Val321Met
NM_001206696.1:c.676G>A NP_001193625.1:p.Val226Met
NM_001206696.2:c.676G>A NP_001193625.1:p.Val226Met
NM_006147.3:c.961G>A NP_006138.1:p.Val321Met
ENST00000367021.7:c.961G>A ENSP00000355988.3:p.Val321Met
ENST00000542854.5:c.676G>A ENSP00000440532.1:p.Val226Met
ENST00000643798.1:c.*471G>A ENSP00000496669.1:n.*471G>A
ENST00000696133.1:c.961G>A ENSP00000512426.1:p.Val321Met
ENST00000696134.1:c.*388G>A ENSP00000512427.1:n.*388G>A