Canonical Allele Identifier: CA2484367623
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209796381T= , CM000663.2:g.209796381T= GRCh38
NC_000001.10:g.209969726T= , CM000663.1:g.209969726T= GRCh37
NC_000001.9:g.208036349T= NCBI36
NG_007081.2:g.14754A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.346A= ENSP00000512426.1:p.Ile116=
ENST00000696134.1:c.346A= ENSP00000512427.1:p.Ile116=
ENST00000367021.8:c.346A= MANE Select ENSP00000355988.3:p.Ile116=
ENST00000643798.1:c.346A= ENSP00000496669.1:p.Ile116=
ENST00000367021.7:c.346A= ENSP00000355988.3:p.Ile116=
ENST00000456314.1:c.346A= ENSP00000403855.1:p.Ile116=
ENST00000542854.5:c.61A= ENSP00000440532.1:p.Ile21=
NM_001206696.1:c.61A= NP_001193625.1:p.Ile21=
NM_006147.3:c.346A= NP_006138.1:p.Ile116=
NM_006147.4:c.346A= MANE Select NP_006138.1:p.Ile116=
NM_001206696.2:c.61A= NP_001193625.1:p.Ile21=