Canonical Allele Identifier: CA423031403

Gene: IRF6

Linked Data

• gnomAD v4: 1-209801321-C-T
• MyVariant Identifiers: chr1:g.209974666C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801321C>T , CM000663.2:g.209801321C>T	GRCh38
NC_000001.10:g.209974666C>T , CM000663.1:g.209974666C>T	GRCh37
NC_000001.9:g.208041289C>T	NCBI36
NG_007081.2:g.9814G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696133.1:c.93G>A	ENSP00000512426.1:p.Arg31=
ENST00000696134.1:c.93G>A	ENSP00000512427.1:p.Arg31=
ENST00000367021.8:c.93G>A MANE Select	ENSP00000355988.3:p.Arg31=
ENST00000643798.1:c.93G>A	ENSP00000496669.1:p.Arg31=
ENST00000367021.7:c.93G>A	ENSP00000355988.3:p.Arg31=
ENST00000456314.1:c.93G>A	ENSP00000403855.1:p.Arg31=
ENST00000542854.5:c.-112+4626G>A	ENSP00000440532.1:n.-112+4626G>A
NM_001206696.1:c.-112+4626G>A	NP_001193625.1:n.-112+4626G>A
NM_006147.3:c.93G>A	NP_006138.1:p.Arg31=
NM_006147.4:c.93G>A MANE Select	NP_006138.1:p.Arg31=
NM_001206696.2:c.-112+4626G>A	NP_001193625.1:n.-112+4626G>A