Canonical Allele Identifier: CA2747565579
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801420_209801421insAAGAGCA , CM000663.2:g.209801420_209801421insAAGAGCA GRCh38
NC_000001.10:g.209974765_209974766insAAGAGCA , CM000663.1:g.209974765_209974766insAAGAGCA GRCh37
NC_000001.9:g.208041388_208041389insAAGAGCA NCBI36
NG_007081.2:g.9714_9715insTGCTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.-3-5_-3-4insTGCTCTT ENSP00000512426.1:n.-3-5_-3-4insTGCTCTT
ENST00000696134.1:c.-3-5_-3-4insTGCTCTT ENSP00000512427.1:n.-3-5_-3-4insTGCTCTT
ENST00000367021.8:c.-3-5_-3-4insTGCTCTT MANE Select ENSP00000355988.3:n.-3-5_-3-4insTGCTCTT
ENST00000643798.1:c.-3-5_-3-4insTGCTCTT ENSP00000496669.1:n.-3-5_-3-4insTGCTCTT
ENST00000367021.7:c.-3-5_-3-4insTGCTCTT ENSP00000355988.3:n.-3-5_-3-4insTGCTCTT
ENST00000456314.1:c.-3-5_-3-4insTGCTCTT ENSP00000403855.1:n.-3-5_-3-4insTGCTCTT
ENST00000542854.5:c.-112+4526_-112+4527insTGCTCTT ENSP00000440532.1:n.-112+4526_-112+4527insTGCTCTT
NM_001206696.1:c.-112+4526_-112+4527insTGCTCTT NP_001193625.1:n.-112+4526_-112+4527insTGCTCTT
NM_006147.3:c.-3-5_-3-4insTGCTCTT NP_006138.1:n.-3-5_-3-4insTGCTCTT
NM_006147.4:c.-3-5_-3-4insTGCTCTT MANE Select NP_006138.1:n.-3-5_-3-4insTGCTCTT
NM_001206696.2:c.-112+4526_-112+4527insTGCTCTT NP_001193625.1:n.-112+4526_-112+4527insTGCTCTT