Canonical Allele Identifier: CA1139923120
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209802047T= , CM000663.2:g.209802047T= GRCh38
NC_000001.10:g.209975392T= , CM000663.1:g.209975392T= GRCh37
NC_000001.9:g.208042015T= NCBI36
NG_007081.2:g.9088A=

Transcript Alleles

HGVS Amino-acid Change
NM_006147.4:c.-75-4A= MANE Select NP_006138.1:n.-75-4A=
ENST00000367021.8:c.-75-4A= MANE Select ENSP00000355988.3:n.-75-4A=
NM_001206696.1:c.-112+3900A= NP_001193625.1:n.-112+3900A=
NM_001206696.2:c.-112+3900A= NP_001193625.1:n.-112+3900A=
NM_006147.3:c.-75-4A= NP_006138.1:n.-75-4A=
ENST00000367021.7:c.-75-4A= ENSP00000355988.3:n.-75-4A=
ENST00000456314.1:c.-79A= ENSP00000403855.1:n.-79A=
ENST00000542854.5:c.-112+3900A= ENSP00000440532.1:n.-112+3900A=
ENST00000696133.1:c.-75-4A= ENSP00000512426.1:n.-75-4A=
ENST00000696134.1:c.-75-4A= ENSP00000512427.1:n.-75-4A=