Canonical Allele Identifier: CA453640084
Gene: FSCN1 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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