Canonical Allele Identifier: CA2484369830
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209802041A>C , CM000663.2:g.209802041A>C GRCh38
NC_000001.10:g.209975386A>C , CM000663.1:g.209975386A>C GRCh37
NC_000001.9:g.208042009A>C NCBI36
NG_007081.2:g.9094T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.-73T>G ENSP00000512426.1:n.-73T>G
ENST00000696134.1:c.-73T>G ENSP00000512427.1:n.-73T>G
ENST00000367021.8:c.-73T>G MANE Select ENSP00000355988.3:n.-73T>G
ENST00000643798.1:c.-73T>G ENSP00000496669.1:n.-73T>G
ENST00000367021.7:c.-73T>G ENSP00000355988.3:n.-73T>G
ENST00000456314.1:c.-73T>G ENSP00000403855.1:n.-73T>G
ENST00000542854.5:c.-112+3906T>G ENSP00000440532.1:n.-112+3906T>G
NM_001206696.1:c.-112+3906T>G NP_001193625.1:n.-112+3906T>G
NM_006147.3:c.-73T>G NP_006138.1:n.-73T>G
NM_006147.4:c.-73T>G MANE Select NP_006138.1:n.-73T>G
NM_001206696.2:c.-112+3906T>G NP_001193625.1:n.-112+3906T>G