Canonical Allele Identifier: CA2484370706
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209804499C>A , CM000663.2:g.209804499C>A GRCh38
NC_000001.10:g.209977844C>A , CM000663.1:g.209977844C>A GRCh37
NC_000001.9:g.208044467C>A NCBI36
NG_007081.2:g.6636G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.-76+1448G>T ENSP00000512426.1:n.-76+1448G>T
ENST00000696134.1:c.-76+1448G>T ENSP00000512427.1:n.-76+1448G>T
ENST00000367021.8:c.-76+1448G>T MANE Select ENSP00000355988.3:n.-76+1448G>T
ENST00000367021.7:c.-76+1448G>T ENSP00000355988.3:n.-76+1448G>T
ENST00000542854.5:c.-112+1448G>T ENSP00000440532.1:n.-112+1448G>T
NM_001206696.1:c.-112+1448G>T NP_001193625.1:n.-112+1448G>T
NM_006147.3:c.-76+1448G>T NP_006138.1:n.-76+1448G>T
NM_006147.4:c.-76+1448G>T MANE Select NP_006138.1:n.-76+1448G>T
NM_001206696.2:c.-112+1448G>T NP_001193625.1:n.-112+1448G>T