Canonical Allele Identifier: CA916393841
Gene: IRF6 HGNC NCBI

Linked Data

dbSNP Id: rs1571976872

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209786107_209786108insC , CM000663.2:g.209786107_209786108insC GRCh38
NC_000001.10:g.209959452_209959453insC , CM000663.1:g.209959452_209959453insC GRCh37
NC_000001.9:g.208026075_208026076insC NCBI36
NG_007081.2:g.25027_25028insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.1400+2316_1400+2317insG ENSP00000512426.1:n.1400+2316_1400+2317insG
ENST00000696134.1:c.*3143_*3144insG ENSP00000512427.1:n.*3143_*3144insG
ENST00000367021.8:c.*2312_*2313insG MANE Select ENSP00000355988.3:n.*2312_*2313insG
ENST00000367021.7:c.*2312_*2313insG ENSP00000355988.3:n.*2312_*2313insG
ENST00000542854.5:c.*2312_*2313insG ENSP00000440532.1:n.*2312_*2313insG
NM_001206696.1:c.*2312_*2313insG NP_001193625.1:n.*2312_*2313insG
NM_006147.3:c.*2312_*2313insG NP_006138.1:n.*2312_*2313insG
NM_006147.4:c.*2312_*2313insG MANE Select NP_006138.1:n.*2312_*2313insG
NM_001206696.2:c.*2312_*2313insG NP_001193625.1:n.*2312_*2313insG