Canonical Allele Identifier: CA1139837604
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209803766A= , CM000663.2:g.209803766A= GRCh38
NC_000001.10:g.209977111A= , CM000663.1:g.209977111A= GRCh37
NC_000001.9:g.208043734A= NCBI36
NG_007081.2:g.7369T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.-75-1723T= ENSP00000512426.1:n.-75-1723T=
ENST00000696134.1:c.-75-1723T= ENSP00000512427.1:n.-75-1723T=
ENST00000367021.8:c.-75-1723T= MANE Select ENSP00000355988.3:n.-75-1723T=
ENST00000367021.7:c.-75-1723T= ENSP00000355988.3:n.-75-1723T=
ENST00000542854.5:c.-112+2181T= ENSP00000440532.1:n.-112+2181T=
NM_001206696.1:c.-112+2181T= NP_001193625.1:n.-112+2181T=
NM_006147.3:c.-75-1723T= NP_006138.1:n.-75-1723T=
NM_006147.4:c.-75-1723T= MANE Select NP_006138.1:n.-75-1723T=
NM_001206696.2:c.-112+2181T= NP_001193625.1:n.-112+2181T=