Canonical Allele Identifier: CA453640075
Gene: FSCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.5643166G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603535G>A , CM000669.2:g.5603535G>A GRCh38
NC_000007.13:g.5643166G>A , CM000669.1:g.5643166G>A GRCh37
NC_000007.12:g.5609692G>A NCBI36
NG_030004.1:g.15731G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.1029G>A MANE Select ENSP00000371798.3:p.Arg343=
ENST00000382361.7:c.1029G>A ENSP00000371798.3:p.Arg343=
ENST00000405801.2:c.195G>A ENSP00000383982.2:p.Arg65=
ENST00000444748.5:c.195G>A ENSP00000404506.1:p.Arg65=
ENST00000447103.5:c.195G>A ENSP00000409967.1:p.Arg65=
ENST00000473330.1:n.582G>A
NM_003088.3:c.1029G>A NP_003079.1:p.Arg343=
NM_003088.4:c.1029G>A MANE Select NP_003079.1:p.Arg343=