Canonical Allele Identifier: CA2484367274
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209795457G= , CM000663.2:g.209795457G= GRCh38
NC_000001.10:g.209968802G= , CM000663.1:g.209968802G= GRCh37
NC_000001.9:g.208035425G= NCBI36
NG_007081.2:g.15678C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.380-39C= ENSP00000512426.1:n.380-39C=
ENST00000696134.1:c.380-39C= ENSP00000512427.1:n.380-39C=
ENST00000367021.8:c.380-39C= MANE Select ENSP00000355988.3:n.380-39C=
ENST00000643798.1:c.380-39C= ENSP00000496669.1:n.380-39C=
ENST00000367021.7:c.380-39C= ENSP00000355988.3:n.380-39C=
ENST00000456314.1:c.380-39C= ENSP00000403855.1:n.380-39C=
ENST00000542854.5:c.95-39C= ENSP00000440532.1:n.95-39C=
NM_001206696.1:c.95-39C= NP_001193625.1:n.95-39C=
NM_006147.3:c.380-39C= NP_006138.1:n.380-39C=
NM_006147.4:c.380-39C= MANE Select NP_006138.1:n.380-39C=
NM_001206696.2:c.95-39C= NP_001193625.1:n.95-39C=