Canonical Allele Identifier: CA453640083
Gene: FSCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.5643169C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603538C>G , CM000669.2:g.5603538C>G GRCh38
NC_000007.13:g.5643169C>G , CM000669.1:g.5643169C>G GRCh37
NC_000007.12:g.5609695C>G NCBI36
NG_030004.1:g.15734C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.1032C>G MANE Select ENSP00000371798.3:p.Arg344=
ENST00000382361.7:c.1032C>G ENSP00000371798.3:p.Arg344=
ENST00000405801.2:c.198C>G ENSP00000383982.2:p.Arg66=
ENST00000444748.5:c.198C>G ENSP00000404506.1:p.Arg66=
ENST00000447103.5:c.198C>G ENSP00000409967.1:p.Arg66=
ENST00000473330.1:n.585C>G
NM_003088.3:c.1032C>G NP_003079.1:p.Arg344=
NM_003088.4:c.1032C>G MANE Select NP_003079.1:p.Arg344=