Canonical Allele Identifier: CA423031395

Gene: IRF6

Linked Data

• MyVariant Identifiers: chr1:g.209974660A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209801315A>G , CM000663.2:g.209801315A>G	GRCh38
NC_000001.10:g.209974660A>G , CM000663.1:g.209974660A>G	GRCh37
NC_000001.9:g.208041283A>G	NCBI36
NG_007081.2:g.9820T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696133.1:c.99T>C	ENSP00000512426.1:p.Ser33=
ENST00000696134.1:c.99T>C	ENSP00000512427.1:p.Ser33=
ENST00000367021.8:c.99T>C MANE Select	ENSP00000355988.3:p.Ser33=
ENST00000643798.1:c.99T>C	ENSP00000496669.1:p.Ser33=
ENST00000367021.7:c.99T>C	ENSP00000355988.3:p.Ser33=
ENST00000456314.1:c.99T>C	ENSP00000403855.1:p.Ser33=
ENST00000542854.5:c.-112+4632T>C	ENSP00000440532.1:n.-112+4632T>C
NM_001206696.1:c.-112+4632T>C	NP_001193625.1:n.-112+4632T>C
NM_006147.3:c.99T>C	NP_006138.1:p.Ser33=
NM_006147.4:c.99T>C MANE Select	NP_006138.1:p.Ser33=
NM_001206696.2:c.-112+4632T>C	NP_001193625.1:n.-112+4632T>C