Canonical Allele Identifier: CA3077250839
Community Standard Title: NM_006147.4(IRF6):c.-3-12T=
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801428A= , CM000663.2:g.209801428A= GRCh38
NC_000001.10:g.209974773A= , CM000663.1:g.209974773A= GRCh37
NC_000001.9:g.208041396A= NCBI36
NG_007081.2:g.9707T=

Transcript Alleles

HGVS Amino-acid Change
NM_006147.4:c.-3-12T= MANE Select NP_006138.1:n.-3-12T=
ENST00000367021.8:c.-3-12T= MANE Select ENSP00000355988.3:n.-3-12T=
NM_001206696.1:c.-112+4519T= NP_001193625.1:n.-112+4519T=
NM_001206696.2:c.-112+4519T= NP_001193625.1:n.-112+4519T=
NM_006147.3:c.-3-12T= NP_006138.1:n.-3-12T=
ENST00000367021.7:c.-3-12T= ENSP00000355988.3:n.-3-12T=
ENST00000456314.1:c.-3-12T= ENSP00000403855.1:n.-3-12T=
ENST00000542854.5:c.-112+4519T= ENSP00000440532.1:n.-112+4519T=
ENST00000643798.1:c.-3-12T= ENSP00000496669.1:n.-3-12T=
ENST00000696133.1:c.-3-12T= ENSP00000512426.1:n.-3-12T=
ENST00000696134.1:c.-3-12T= ENSP00000512427.1:n.-3-12T=