Canonical Allele Identifier: CA2841866824
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801325dup , CM000663.2:g.209801325dup GRCh38
NC_000001.10:g.209974670dup , CM000663.1:g.209974670dup GRCh37
NC_000001.9:g.208041293dup NCBI36
NG_007081.2:g.9810dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.89dup ENSP00000512426.1:p.His30GlnfsTer5
ENST00000696134.1:c.89dup ENSP00000512427.1:p.His30GlnfsTer5
ENST00000367021.8:c.89dup MANE Select ENSP00000355988.3:p.His30GlnfsTer5
ENST00000643798.1:c.89dup ENSP00000496669.1:p.His30GlnfsTer5
ENST00000367021.7:c.89dup ENSP00000355988.3:p.His30GlnfsTer5
ENST00000456314.1:c.89dup ENSP00000403855.1:p.His30GlnfsTer5
ENST00000542854.5:c.-112+4622dup ENSP00000440532.1:n.-112+4622dup
NM_001206696.1:c.-112+4622dup NP_001193625.1:n.-112+4622dup
NM_006147.3:c.89dup NP_006138.1:p.His30GlnfsTer5
NM_006147.4:c.89dup MANE Select NP_006138.1:p.His30GlnfsTer5
NM_001206696.2:c.-112+4622dup NP_001193625.1:n.-112+4622dup