Canonical Allele Identifier: CA2484364025
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209786109_209786110delinsAG , CM000663.2:g.209786109_209786110delinsAG GRCh38
NC_000001.10:g.209959454_209959455delinsAG , CM000663.1:g.209959454_209959455delinsAG GRCh37
NC_000001.9:g.208026077_208026078delinsAG NCBI36
NG_007081.2:g.25025_25026delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1400+2314_1400+2315delinsCT ENSP00000512426.1:n.1400+2314_1400+2315delinsCT
ENST00000696134.1:c.*3141_*3142delinsCT ENSP00000512427.1:n.*3141_*3142delinsCT
ENST00000367021.8:c.*2310_*2311delinsCT MANE Select ENSP00000355988.3:n.*2310_*2311delinsCT
ENST00000367021.7:c.*2310_*2311delinsCT ENSP00000355988.3:n.*2310_*2311delinsCT
ENST00000542854.5:c.*2310_*2311delinsCT ENSP00000440532.1:n.*2310_*2311delinsCT
NM_001206696.1:c.*2310_*2311delinsCT NP_001193625.1:n.*2310_*2311delinsCT
NM_006147.3:c.*2310_*2311delinsCT NP_006138.1:n.*2310_*2311delinsCT
NM_006147.4:c.*2310_*2311delinsCT MANE Select NP_006138.1:n.*2310_*2311delinsCT
NM_001206696.2:c.*2310_*2311delinsCT NP_001193625.1:n.*2310_*2311delinsCT