Canonical Allele Identifier: CA1377234
Community Standard Title: NM_006147.4(IRF6):c.921C>T (p.Ser307=)
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209790634G>A , CM000663.2:g.209790634G>A GRCh38
NC_000001.10:g.209963979G>A , CM000663.1:g.209963979G>A GRCh37
NC_000001.9:g.208030602G>A NCBI36
NG_007081.2:g.20501C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006147.4:c.921C>T MANE Select NP_006138.1:p.Ser307=
ENST00000367021.8:c.921C>T MANE Select ENSP00000355988.3:p.Ser307=
NM_001206696.1:c.636C>T NP_001193625.1:p.Ser212=
NM_001206696.2:c.636C>T NP_001193625.1:p.Ser212=
NM_006147.3:c.921C>T NP_006138.1:p.Ser307=
ENST00000367021.7:c.921C>T ENSP00000355988.3:p.Ser307=
ENST00000542854.5:c.636C>T ENSP00000440532.1:p.Ser212=
ENST00000643798.1:c.*431C>T ENSP00000496669.1:n.*431C>T
ENST00000696133.1:c.921C>T ENSP00000512426.1:p.Ser307=
ENST00000696134.1:c.*348C>T ENSP00000512427.1:n.*348C>T