Canonical Allele Identifier: CA344577554
Community Standard Title: NM_006147.4(IRF6):c.748C>T (p.Arg250Ter)
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209790807G>A , CM000663.2:g.209790807G>A GRCh38
NC_000001.10:g.209964152G>A , CM000663.1:g.209964152G>A GRCh37
NC_000001.9:g.208030775G>A NCBI36
NG_007081.2:g.20328C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006147.4:c.748C>T MANE Select NP_006138.1:p.Arg250Ter
ENST00000367021.8:c.748C>T MANE Select ENSP00000355988.3:p.Arg250Ter
NM_001206696.1:c.463C>T NP_001193625.1:p.Arg155Ter
NM_001206696.2:c.463C>T NP_001193625.1:p.Arg155Ter
NM_006147.3:c.748C>T NP_006138.1:p.Arg250Ter
ENST00000367021.7:c.748C>T ENSP00000355988.3:p.Arg250Ter
ENST00000456314.1:c.748C>T ENSP00000403855.1:p.Arg250Ter
ENST00000464698.1:n.527C>T
ENST00000542854.5:c.463C>T ENSP00000440532.1:p.Arg155Ter
ENST00000643798.1:c.*258C>T ENSP00000496669.1:n.*258C>T
ENST00000696133.1:c.748C>T ENSP00000512426.1:p.Arg250Ter
ENST00000696134.1:c.*175C>T ENSP00000512427.1:n.*175C>T