Canonical Allele Identifier: CA2484369465

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801086_209801087delinsCA , CM000663.2:g.209801086_209801087delinsCA	GRCh38
NC_000001.10:g.209974431_209974432delinsCA , CM000663.1:g.209974431_209974432delinsCA	GRCh37
NC_000001.9:g.208041054_208041055delinsCA	NCBI36
NG_007081.2:g.10048_10049delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.174+153_174+154delinsTG	ENSP00000512426.1:n.174+153_174+154delinsTG
ENST00000696134.1:c.174+153_174+154delinsTG	ENSP00000512427.1:n.174+153_174+154delinsTG
ENST00000367021.8:c.174+153_174+154delinsTG MANE Select	ENSP00000355988.3:n.174+153_174+154delinsTG
ENST00000643798.1:c.174+153_174+154delinsTG	ENSP00000496669.1:n.174+153_174+154delinsTG
ENST00000367021.7:c.174+153_174+154delinsTG	ENSP00000355988.3:n.174+153_174+154delinsTG
ENST00000456314.1:c.174+153_174+154delinsTG	ENSP00000403855.1:n.174+153_174+154delinsTG
ENST00000542854.5:c.-111-4535_-111-4534delinsTG	ENSP00000440532.1:n.-111-4535_-111-4534delinsTG
NM_001206696.1:c.-111-4535_-111-4534delinsTG	NP_001193625.1:n.-111-4535_-111-4534delinsTG
NM_006147.3:c.174+153_174+154delinsTG	NP_006138.1:n.174+153_174+154delinsTG
NM_006147.4:c.174+153_174+154delinsTG MANE Select	NP_006138.1:n.174+153_174+154delinsTG
NM_001206696.2:c.-111-4535_-111-4534delinsTG	NP_001193625.1:n.-111-4535_-111-4534delinsTG