Canonical Allele Identifier: CA1011779874

Gene: IRF6

Linked Data

• dbSNP Id: rs2077938906
• gnomAD v3: 1-209801182-C-CAA
• gnomAD v4: 1-209801182-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801182_209801183insAA , CM000663.2:g.209801182_209801183insAA	GRCh38
NC_000001.10:g.209974527_209974528insAA , CM000663.1:g.209974527_209974528insAA	GRCh37
NC_000001.9:g.208041150_208041151insAA	NCBI36
NG_007081.2:g.9952_9953insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.174+57_174+58insTT	ENSP00000512426.1:n.174+57_174+58insTT
ENST00000696134.1:c.174+57_174+58insTT	ENSP00000512427.1:n.174+57_174+58insTT
ENST00000367021.8:c.174+57_174+58insTT MANE Select	ENSP00000355988.3:n.174+57_174+58insTT
ENST00000643798.1:c.174+57_174+58insTT	ENSP00000496669.1:n.174+57_174+58insTT
ENST00000367021.7:c.174+57_174+58insTT	ENSP00000355988.3:n.174+57_174+58insTT
ENST00000456314.1:c.174+57_174+58insTT	ENSP00000403855.1:n.174+57_174+58insTT
ENST00000542854.5:c.-111-4631_-111-4630insTT	ENSP00000440532.1:n.-111-4631_-111-4630insTT
NM_001206696.1:c.-111-4631_-111-4630insTT	NP_001193625.1:n.-111-4631_-111-4630insTT
NM_006147.3:c.174+57_174+58insTT	NP_006138.1:n.174+57_174+58insTT
NM_006147.4:c.174+57_174+58insTT MANE Select	NP_006138.1:n.174+57_174+58insTT
NM_001206696.2:c.-111-4631_-111-4630insTT	NP_001193625.1:n.-111-4631_-111-4630insTT