Canonical Allele Identifier: CA2484367119
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209795055T= , CM000663.2:g.209795055T= GRCh38
NC_000001.10:g.209968400T= , CM000663.1:g.209968400T= GRCh37
NC_000001.9:g.208035023T= NCBI36
NG_007081.2:g.16080A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.508+235A= ENSP00000512426.1:n.508+235A=
ENST00000696134.1:c.508+235A= ENSP00000512427.1:n.508+235A=
ENST00000367021.8:c.508+235A= MANE Select ENSP00000355988.3:n.508+235A=
ENST00000643798.1:c.508+235A= ENSP00000496669.1:n.508+235A=
ENST00000367021.7:c.508+235A= ENSP00000355988.3:n.508+235A=
ENST00000456314.1:c.508+235A= ENSP00000403855.1:n.508+235A=
ENST00000542854.5:c.223+235A= ENSP00000440532.1:n.223+235A=
NM_001206696.1:c.223+235A= NP_001193625.1:n.223+235A=
NM_006147.3:c.508+235A= NP_006138.1:n.508+235A=
NM_006147.4:c.508+235A= MANE Select NP_006138.1:n.508+235A=
NM_001206696.2:c.223+235A= NP_001193625.1:n.223+235A=