Canonical Allele Identifier: CA2484365202
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209789597C= , CM000663.2:g.209789597C= GRCh38
NC_000001.10:g.209962942C= , CM000663.1:g.209962942C= GRCh37
NC_000001.9:g.208029565C= NCBI36
NG_007081.2:g.21538G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696133.1:c.1179+70G= ENSP00000512426.1:n.1179+70G=
ENST00000696134.1:c.*606+70G= ENSP00000512427.1:n.*606+70G=
ENST00000367021.8:c.1179+70G= MANE Select ENSP00000355988.3:n.1179+70G=
ENST00000643798.1:c.*689+70G= ENSP00000496669.1:n.*689+70G=
ENST00000367021.7:c.1179+70G= ENSP00000355988.3:n.1179+70G=
ENST00000542854.5:c.894+70G= ENSP00000440532.1:n.894+70G=
NM_001206696.1:c.894+70G= NP_001193625.1:n.894+70G=
NM_006147.3:c.1179+70G= NP_006138.1:n.1179+70G=
NM_006147.4:c.1179+70G= MANE Select NP_006138.1:n.1179+70G=
NM_001206696.2:c.894+70G= NP_001193625.1:n.894+70G=