Canonical Allele Identifier: CA1139908281
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209795339C= , CM000663.2:g.209795339C= GRCh38
NC_000001.10:g.209968684C= , CM000663.1:g.209968684C= GRCh37
NC_000001.9:g.208035307C= NCBI36
NG_007081.2:g.15796G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.459G= ENSP00000512426.1:p.Ser153=
ENST00000696134.1:c.459G= ENSP00000512427.1:p.Ser153=
ENST00000367021.8:c.459G= MANE Select ENSP00000355988.3:p.Ser153=
ENST00000643798.1:c.459G= ENSP00000496669.1:p.Ser153=
ENST00000367021.7:c.459G= ENSP00000355988.3:p.Ser153=
ENST00000456314.1:c.459G= ENSP00000403855.1:p.Ser153=
ENST00000542854.5:c.174G= ENSP00000440532.1:p.Ser58=
NM_001206696.1:c.174G= NP_001193625.1:p.Ser58=
NM_006147.3:c.459G= NP_006138.1:p.Ser153=
NM_006147.4:c.459G= MANE Select NP_006138.1:p.Ser153=
NM_001206696.2:c.174G= NP_001193625.1:p.Ser58=