Canonical Allele Identifier: CA36754488
Gene: IRF6 HGNC NCBI

Linked Data

dbSNP Id: rs1024327039

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209795353C>T , CM000663.2:g.209795353C>T GRCh38
NC_000001.10:g.209968698C>T , CM000663.1:g.209968698C>T GRCh37
NC_000001.9:g.208035321C>T NCBI36
NG_007081.2:g.15782G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.445G>A ENSP00000512426.1:p.Glu149Lys
ENST00000696134.1:c.445G>A ENSP00000512427.1:p.Glu149Lys
ENST00000367021.8:c.445G>A MANE Select ENSP00000355988.3:p.Glu149Lys
ENST00000643798.1:c.445G>A ENSP00000496669.1:p.Glu149Lys
ENST00000367021.7:c.445G>A ENSP00000355988.3:p.Glu149Lys
ENST00000456314.1:c.445G>A ENSP00000403855.1:p.Glu149Lys
ENST00000542854.5:c.160G>A ENSP00000440532.1:p.Glu54Lys
NM_001206696.1:c.160G>A NP_001193625.1:p.Glu54Lys
NM_006147.3:c.445G>A NP_006138.1:p.Glu149Lys
NM_006147.4:c.445G>A MANE Select NP_006138.1:p.Glu149Lys
NM_001206696.2:c.160G>A NP_001193625.1:p.Glu54Lys