Canonical Allele Identifier: CA2650336306

Gene: IRF6

Linked Data

• gnomAD v4: 1-209795230-CAAGGTCAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209795233_209795240del , CM000663.2:g.209795233_209795240del	GRCh38
NC_000001.10:g.209968578_209968585del , CM000663.1:g.209968578_209968585del	GRCh37
NC_000001.9:g.208035201_208035208del	NCBI36
NG_007081.2:g.15897_15904del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696133.1:c.508+52_508+59del	ENSP00000512426.1:n.508+52_508+59del
ENST00000696134.1:c.508+52_508+59del	ENSP00000512427.1:n.508+52_508+59del
ENST00000367021.8:c.508+52_508+59del MANE Select	ENSP00000355988.3:n.508+52_508+59del
ENST00000643798.1:c.508+52_508+59del	ENSP00000496669.1:n.508+52_508+59del
ENST00000367021.7:c.508+52_508+59del	ENSP00000355988.3:n.508+52_508+59del
ENST00000456314.1:c.508+52_508+59del	ENSP00000403855.1:n.508+52_508+59del
ENST00000542854.5:c.223+52_223+59del	ENSP00000440532.1:n.223+52_223+59del
NM_001206696.1:c.223+52_223+59del	NP_001193625.1:n.223+52_223+59del
NM_006147.3:c.508+52_508+59del	NP_006138.1:n.508+52_508+59del
NM_006147.4:c.508+52_508+59del MANE Select	NP_006138.1:n.508+52_508+59del
NM_001206696.2:c.223+52_223+59del	NP_001193625.1:n.223+52_223+59del