Canonical Allele Identifier: CA730852047

Gene: IRF6

Linked Data

• dbSNP Id: rs1293465544
• MyVariant Identifiers: chr1:g.209959236C>T (hg19) ; chr1:g.209785891C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209785891C>T , CM000663.2:g.209785891C>T	GRCh38
NC_000001.10:g.209959236C>T , CM000663.1:g.209959236C>T	GRCh37
NC_000001.9:g.208025859C>T	NCBI36
NG_007081.2:g.25244G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.1401-2182G>A	ENSP00000512426.1:n.1401-2182G>A
ENST00000696134.1:c.*3360G>A	ENSP00000512427.1:n.*3360G>A
ENST00000367021.8:c.*2529G>A MANE Select	ENSP00000355988.3:n.*2529G>A
ENST00000367021.7:c.*2529G>A	ENSP00000355988.3:n.*2529G>A
ENST00000542854.5:c.*2529G>A	ENSP00000440532.1:n.*2529G>A
NM_001206696.1:c.*2529G>A	NP_001193625.1:n.*2529G>A
NM_006147.3:c.*2529G>A	NP_006138.1:n.*2529G>A
NM_006147.4:c.*2529G>A MANE Select	NP_006138.1:n.*2529G>A
NM_001206696.2:c.*2529G>A	NP_001193625.1:n.*2529G>A