Canonical Allele Identifier: CA2747567903
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209786247_209786249del , CM000663.2:g.209786247_209786249del GRCh38
NC_000001.10:g.209959592_209959594del , CM000663.1:g.209959592_209959594del GRCh37
NC_000001.9:g.208026215_208026217del NCBI36
NG_007081.2:g.24886_24888del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1400+2175_1400+2177del ENSP00000512426.1:n.1400+2175_1400+2177del
ENST00000696134.1:c.*3002_*3004del ENSP00000512427.1:n.*3002_*3004del
ENST00000367021.8:c.*2171_*2173del MANE Select ENSP00000355988.3:n.*2171_*2173del
ENST00000367021.7:c.*2171_*2173del ENSP00000355988.3:n.*2171_*2173del
ENST00000542854.5:c.*2171_*2173del ENSP00000440532.1:n.*2171_*2173del
NM_001206696.1:c.*2171_*2173del NP_001193625.1:n.*2171_*2173del
NM_006147.3:c.*2171_*2173del NP_006138.1:n.*2171_*2173del
NM_006147.4:c.*2171_*2173del MANE Select NP_006138.1:n.*2171_*2173del
NM_001206696.2:c.*2171_*2173del NP_001193625.1:n.*2171_*2173del