Canonical Allele Identifier: CA4147504
Gene: FSCN1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1640233

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603514T>C , CM000669.2:g.5603514T>C GRCh38
NC_000007.13:g.5643145T>C , CM000669.1:g.5643145T>C GRCh37
NC_000007.12:g.5609671T>C NCBI36
NG_030004.1:g.15710T>C

Transcript Alleles

HGVS Amino-acid change
NM_003088.3:c.1008T>C VV NP_003079.1:p.Phe336=
NM_003088.4:c.1008T>C VV MANE Preferred NP_003079.1:p.Phe336=
ENST00000382361.7:c.1008T>C ENSP00000371798.3:p.Phe336=
ENST00000405801.2:c.174T>C ENSP00000383982.2:p.Phe58=
ENST00000444748.5:c.174T>C ENSP00000404506.1:p.Phe58=
ENST00000447103.5:c.174T>C ENSP00000409967.1:p.Phe58=
ENST00000473330.1:n.561T>C