Canonical Allele Identifier: CA2484369567

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801304_209801306delinsTGG , CM000663.2:g.209801304_209801306delinsTGG	GRCh38
NC_000001.10:g.209974649_209974651delinsTGG , CM000663.1:g.209974649_209974651delinsTGG	GRCh37
NC_000001.9:g.208041272_208041274delinsTGG	NCBI36
NG_007081.2:g.9829_9831delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.108_110delinsCCA	ENSP00000512426.1:p.Phe36=
ENST00000696134.1:c.108_110delinsCCA	ENSP00000512427.1:p.Phe36=
ENST00000367021.8:c.108_110delinsCCA MANE Select	ENSP00000355988.3:p.Phe36=
ENST00000643798.1:c.108_110delinsCCA	ENSP00000496669.1:p.Phe36=
ENST00000367021.7:c.108_110delinsCCA	ENSP00000355988.3:p.Phe36=
ENST00000456314.1:c.108_110delinsCCA	ENSP00000403855.1:p.Phe36=
ENST00000542854.5:c.-112+4641_-112+4643delinsCCA	ENSP00000440532.1:n.-112+4641_-112+4643delinsCCA
NM_001206696.1:c.-112+4641_-112+4643delinsCCA	NP_001193625.1:n.-112+4641_-112+4643delinsCCA
NM_006147.3:c.108_110delinsCCA	NP_006138.1:p.Phe36=
NM_006147.4:c.108_110delinsCCA MANE Select	NP_006138.1:p.Phe36=
NM_001206696.2:c.-112+4641_-112+4643delinsCCA	NP_001193625.1:n.-112+4641_-112+4643delinsCCA