Canonical Allele Identifier: CA2484369500
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801174T= , CM000663.2:g.209801174T= GRCh38
NC_000001.10:g.209974519T= , CM000663.1:g.209974519T= GRCh37
NC_000001.9:g.208041142T= NCBI36
NG_007081.2:g.9961A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.174+66A= ENSP00000512426.1:n.174+66A=
ENST00000696134.1:c.174+66A= ENSP00000512427.1:n.174+66A=
ENST00000367021.8:c.174+66A= MANE Select ENSP00000355988.3:n.174+66A=
ENST00000643798.1:c.174+66A= ENSP00000496669.1:n.174+66A=
ENST00000367021.7:c.174+66A= ENSP00000355988.3:n.174+66A=
ENST00000456314.1:c.174+66A= ENSP00000403855.1:n.174+66A=
ENST00000542854.5:c.-111-4622A= ENSP00000440532.1:n.-111-4622A=
NM_001206696.1:c.-111-4622A= NP_001193625.1:n.-111-4622A=
NM_006147.3:c.174+66A= NP_006138.1:n.174+66A=
NM_006147.4:c.174+66A= MANE Select NP_006138.1:n.174+66A=
NM_001206696.2:c.-111-4622A= NP_001193625.1:n.-111-4622A=