Canonical Allele Identifier: CA2484364800
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209788532T= , CM000663.2:g.209788532T= GRCh38
NC_000001.10:g.209961877T= , CM000663.1:g.209961877T= GRCh37
NC_000001.9:g.208028500T= NCBI36
NG_007081.2:g.22603A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.1292A= ENSP00000512426.1:p.Asn431=
ENST00000696134.1:c.*719A= ENSP00000512427.1:n.*719A=
ENST00000367021.8:c.1292A= MANE Select ENSP00000355988.3:p.Asn431=
ENST00000643798.1:c.*802A= ENSP00000496669.1:n.*802A=
ENST00000367021.7:c.1292A= ENSP00000355988.3:p.Asn431=
ENST00000542854.5:c.1007A= ENSP00000440532.1:p.Asn336=
NM_001206696.1:c.1007A= NP_001193625.1:p.Asn336=
NM_006147.3:c.1292A= NP_006138.1:p.Asn431=
NM_006147.4:c.1292A= MANE Select NP_006138.1:p.Asn431=
NM_001206696.2:c.1007A= NP_001193625.1:p.Asn336=