Canonical Allele Identifier: CA423030161

Gene: IRF6

Linked Data

• MyVariant Identifiers: chr1:g.209968762T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209795417T>G , CM000663.2:g.209795417T>G	GRCh38
NC_000001.10:g.209968762T>G , CM000663.1:g.209968762T>G	GRCh37
NC_000001.9:g.208035385T>G	NCBI36
NG_007081.2:g.15718A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696133.1:c.381A>C	ENSP00000512426.1:p.Gly127=
ENST00000696134.1:c.381A>C	ENSP00000512427.1:p.Gly127=
ENST00000367021.8:c.381A>C MANE Select	ENSP00000355988.3:p.Gly127=
ENST00000643798.1:c.381A>C	ENSP00000496669.1:p.Gly127=
ENST00000367021.7:c.381A>C	ENSP00000355988.3:p.Gly127=
ENST00000456314.1:c.381A>C	ENSP00000403855.1:p.Gly127=
ENST00000542854.5:c.96A>C	ENSP00000440532.1:p.Gly32=
NM_001206696.1:c.96A>C	NP_001193625.1:p.Gly32=
NM_006147.3:c.381A>C	NP_006138.1:p.Gly127=
NM_006147.4:c.381A>C MANE Select	NP_006138.1:p.Gly127=
NM_001206696.2:c.96A>C	NP_001193625.1:p.Gly32=