Canonical Allele Identifier: CA2484367142

Gene: IRF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209795126_209795127delinsAG , CM000663.2:g.209795126_209795127delinsAG	GRCh38
NC_000001.10:g.209968471_209968472delinsAG , CM000663.1:g.209968471_209968472delinsAG	GRCh37
NC_000001.9:g.208035094_208035095delinsAG	NCBI36
NG_007081.2:g.16008_16009delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.508+163_508+164delinsCT	ENSP00000512426.1:n.508+163_508+164delinsCT
ENST00000696134.1:c.508+163_508+164delinsCT	ENSP00000512427.1:n.508+163_508+164delinsCT
ENST00000367021.8:c.508+163_508+164delinsCT MANE Select	ENSP00000355988.3:n.508+163_508+164delinsCT
ENST00000643798.1:c.508+163_508+164delinsCT	ENSP00000496669.1:n.508+163_508+164delinsCT
ENST00000367021.7:c.508+163_508+164delinsCT	ENSP00000355988.3:n.508+163_508+164delinsCT
ENST00000456314.1:c.508+163_508+164delinsCT	ENSP00000403855.1:n.508+163_508+164delinsCT
ENST00000542854.5:c.223+163_223+164delinsCT	ENSP00000440532.1:n.223+163_223+164delinsCT
NM_001206696.1:c.223+163_223+164delinsCT	NP_001193625.1:n.223+163_223+164delinsCT
NM_006147.3:c.508+163_508+164delinsCT	NP_006138.1:n.508+163_508+164delinsCT
NM_006147.4:c.508+163_508+164delinsCT MANE Select	NP_006138.1:n.508+163_508+164delinsCT
NM_001206696.2:c.223+163_223+164delinsCT	NP_001193625.1:n.223+163_223+164delinsCT