Canonical Allele Identifier: CA2650336200
Gene: IRF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801195_209801196insT , CM000663.2:g.209801195_209801196insT GRCh38
NC_000001.10:g.209974540_209974541insT , CM000663.1:g.209974540_209974541insT GRCh37
NC_000001.9:g.208041163_208041164insT NCBI36
NG_007081.2:g.9939_9940insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.174+44_174+45insA ENSP00000512426.1:n.174+44_174+45insA
ENST00000696134.1:c.174+44_174+45insA ENSP00000512427.1:n.174+44_174+45insA
ENST00000367021.8:c.174+44_174+45insA MANE Select ENSP00000355988.3:n.174+44_174+45insA
ENST00000643798.1:c.174+44_174+45insA ENSP00000496669.1:n.174+44_174+45insA
ENST00000367021.7:c.174+44_174+45insA ENSP00000355988.3:n.174+44_174+45insA
ENST00000456314.1:c.174+44_174+45insA ENSP00000403855.1:n.174+44_174+45insA
ENST00000542854.5:c.-111-4644_-111-4643insA ENSP00000440532.1:n.-111-4644_-111-4643insA
NM_001206696.1:c.-111-4644_-111-4643insA NP_001193625.1:n.-111-4644_-111-4643insA
NM_006147.3:c.174+44_174+45insA NP_006138.1:n.174+44_174+45insA
NM_006147.4:c.174+44_174+45insA MANE Select NP_006138.1:n.174+44_174+45insA
NM_001206696.2:c.-111-4644_-111-4643insA NP_001193625.1:n.-111-4644_-111-4643insA