Canonical Allele Identifier: CA344583097
Community Standard Title: NM_006147.4(IRF6):c.292G>C (p.Asp98His)
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209796435C>G , CM000663.2:g.209796435C>G GRCh38
NC_000001.10:g.209969780C>G , CM000663.1:g.209969780C>G GRCh37
NC_000001.9:g.208036403C>G NCBI36
NG_007081.2:g.14700G>C

Transcript Alleles

HGVS Amino-acid Change
NM_006147.4:c.292G>C MANE Select NP_006138.1:p.Asp98His
ENST00000367021.8:c.292G>C MANE Select ENSP00000355988.3:p.Asp98His
NM_001206696.1:c.7G>C NP_001193625.1:p.Asp3His
NM_001206696.2:c.7G>C NP_001193625.1:p.Asp3His
NM_006147.3:c.292G>C NP_006138.1:p.Asp98His
ENST00000367021.7:c.292G>C ENSP00000355988.3:p.Asp98His
ENST00000456314.1:c.292G>C ENSP00000403855.1:p.Asp98His
ENST00000542854.5:c.7G>C ENSP00000440532.1:p.Asp3His
ENST00000643798.1:c.292G>C ENSP00000496669.1:p.Asp98His
ENST00000696133.1:c.292G>C ENSP00000512426.1:p.Asp98His
ENST00000696134.1:c.292G>C ENSP00000512427.1:p.Asp98His