Canonical Allele Identifier: CA2586964593
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801408_209801409delinsAC , CM000663.2:g.209801408_209801409delinsAC GRCh38
NC_000001.10:g.209974753_209974754delinsAC , CM000663.1:g.209974753_209974754delinsAC GRCh37
NC_000001.9:g.208041376_208041377delinsAC NCBI36
NG_007081.2:g.9726_9727delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.5_6delinsGT ENSP00000512426.1:p.Ala2Gly
ENST00000696134.1:c.5_6delinsGT ENSP00000512427.1:p.Ala2Gly
ENST00000367021.8:c.5_6delinsGT MANE Select ENSP00000355988.3:p.Ala2Gly
ENST00000643798.1:c.5_6delinsGT ENSP00000496669.1:p.Ala2Gly
ENST00000367021.7:c.5_6delinsGT ENSP00000355988.3:p.Ala2Gly
ENST00000456314.1:c.5_6delinsGT ENSP00000403855.1:p.Ala2Gly
ENST00000542854.5:c.-112+4538_-112+4539delinsGT ENSP00000440532.1:n.-112+4538_-112+4539delinsGT
NM_001206696.1:c.-112+4538_-112+4539delinsGT NP_001193625.1:n.-112+4538_-112+4539delinsGT
NM_006147.3:c.5_6delinsGT NP_006138.1:p.Ala2Gly
NM_006147.4:c.5_6delinsGT MANE Select NP_006138.1:p.Ala2Gly
NM_001206696.2:c.-112+4538_-112+4539delinsGT NP_001193625.1:n.-112+4538_-112+4539delinsGT