Canonical Allele Identifier: CA1142124110
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209785975_209785976delinsAA , CM000663.2:g.209785975_209785976delinsAA GRCh38
NC_000001.10:g.209959320_209959321delinsAA , CM000663.1:g.209959320_209959321delinsAA GRCh37
NC_000001.9:g.208025943_208025944delinsAA NCBI36
NG_007081.2:g.25159_25160delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1401-2267_1401-2266delinsTT ENSP00000512426.1:n.1401-2267_1401-2266delinsTT
ENST00000696134.1:c.*3275_*3276delinsTT ENSP00000512427.1:n.*3275_*3276delinsTT
ENST00000367021.8:c.*2444_*2445delinsTT MANE Select ENSP00000355988.3:n.*2444_*2445delinsTT
ENST00000367021.7:c.*2444_*2445delinsTT ENSP00000355988.3:n.*2444_*2445delinsTT
ENST00000542854.5:c.*2444_*2445delinsTT ENSP00000440532.1:n.*2444_*2445delinsTT
NM_001206696.1:c.*2444_*2445delinsTT NP_001193625.1:n.*2444_*2445delinsTT
NM_006147.3:c.*2444_*2445delinsTT NP_006138.1:n.*2444_*2445delinsTT
NM_006147.4:c.*2444_*2445delinsTT MANE Select NP_006138.1:n.*2444_*2445delinsTT
NM_001206696.2:c.*2444_*2445delinsTT NP_001193625.1:n.*2444_*2445delinsTT