Canonical Allele Identifier: CA2484367223
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209795316T= , CM000663.2:g.209795316T= GRCh38
NC_000001.10:g.209968661T= , CM000663.1:g.209968661T= GRCh37
NC_000001.9:g.208035284T= NCBI36
NG_007081.2:g.15819A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.482A= ENSP00000512426.1:p.Asp161=
ENST00000696134.1:c.482A= ENSP00000512427.1:p.Asp161=
ENST00000367021.8:c.482A= MANE Select ENSP00000355988.3:p.Asp161=
ENST00000643798.1:c.482A= ENSP00000496669.1:p.Asp161=
ENST00000367021.7:c.482A= ENSP00000355988.3:p.Asp161=
ENST00000456314.1:c.482A= ENSP00000403855.1:p.Asp161=
ENST00000542854.5:c.197A= ENSP00000440532.1:p.Asp66=
NM_001206696.1:c.197A= NP_001193625.1:p.Asp66=
NM_006147.3:c.482A= NP_006138.1:p.Asp161=
NM_006147.4:c.482A= MANE Select NP_006138.1:p.Asp161=
NM_001206696.2:c.197A= NP_001193625.1:p.Asp66=