Canonical Allele Identifier: CA2484363809

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209785735_209785737delinsCTG , CM000663.2:g.209785735_209785737delinsCTG	GRCh38
NC_000001.10:g.209959080_209959082delinsCTG , CM000663.1:g.209959080_209959082delinsCTG	GRCh37
NC_000001.9:g.208025703_208025705delinsCTG	NCBI36
NG_007081.2:g.25398_25400delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.1401-2028_1401-2026delinsCAG	ENSP00000512426.1:n.1401-2028_1401-2026delinsCAG
ENST00000696134.1:c.*3514_*3516delinsCAG	ENSP00000512427.1:n.*3514_*3516delinsCAG
ENST00000367021.8:c.*2683_*2685delinsCAG MANE Select	ENSP00000355988.3:n.*2683_*2685delinsCAG
ENST00000367021.7:c.*2683_*2685delinsCAG	ENSP00000355988.3:n.*2683_*2685delinsCAG
ENST00000542854.5:c.*2683_*2685delinsCAG	ENSP00000440532.1:n.*2683_*2685delinsCAG
NM_001206696.1:c.*2683_*2685delinsCAG	NP_001193625.1:n.*2683_*2685delinsCAG
NM_006147.3:c.*2683_*2685delinsCAG	NP_006138.1:n.*2683_*2685delinsCAG
NM_006147.4:c.*2683_*2685delinsCAG MANE Select	NP_006138.1:n.*2683_*2685delinsCAG
NM_001206696.2:c.*2683_*2685delinsCAG	NP_001193625.1:n.*2683_*2685delinsCAG