Canonical Allele Identifier: CA344585906

Gene: IRF6

Linked Data

• ClinVar Variation Id: 3061358
• ClinVar RCV Id: RCV004554970
• MyVariant Identifiers: chr1:g.209974697C>T (hg19) ; chr1:g.209801352C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801352C>T , CM000663.2:g.209801352C>T	GRCh38
NC_000001.10:g.209974697C>T , CM000663.1:g.209974697C>T	GRCh37
NC_000001.9:g.208041320C>T	NCBI36
NG_007081.2:g.9783G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.62G>A	ENSP00000512426.1:p.Gly21Asp
ENST00000696134.1:c.62G>A	ENSP00000512427.1:p.Gly21Asp
ENST00000367021.8:c.62G>A MANE Select	ENSP00000355988.3:p.Gly21Asp
ENST00000643798.1:c.62G>A	ENSP00000496669.1:p.Gly21Asp
ENST00000367021.7:c.62G>A	ENSP00000355988.3:p.Gly21Asp
ENST00000456314.1:c.62G>A	ENSP00000403855.1:p.Gly21Asp
ENST00000542854.5:c.-112+4595G>A	ENSP00000440532.1:n.-112+4595G>A
NM_001206696.1:c.-112+4595G>A	NP_001193625.1:n.-112+4595G>A
NM_006147.3:c.62G>A	NP_006138.1:p.Gly21Asp
NM_006147.4:c.62G>A MANE Select	NP_006138.1:p.Gly21Asp
NM_001206696.2:c.-112+4595G>A	NP_001193625.1:n.-112+4595G>A