Canonical Allele Identifier: CA366723172
Gene: FSCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.5642935T>A (hg19) chr7:g.5603304T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603304T>A , CM000669.2:g.5603304T>A GRCh38
NC_000007.13:g.5642935T>A , CM000669.1:g.5642935T>A GRCh37
NC_000007.12:g.5609461T>A NCBI36
NG_030004.1:g.15500T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.880T>A MANE Select ENSP00000371798.3:p.Phe294Ile
ENST00000382361.7:c.880T>A ENSP00000371798.3:p.Phe294Ile
ENST00000405801.2:c.46T>A ENSP00000383982.2:p.Phe16Ile
ENST00000444748.5:c.46T>A ENSP00000404506.1:p.Phe16Ile
ENST00000447103.5:c.46T>A ENSP00000409967.1:p.Phe16Ile
ENST00000473330.1:n.433T>A
NM_003088.3:c.880T>A NP_003079.1:p.Phe294Ile
NM_003088.4:c.880T>A MANE Select NP_003079.1:p.Phe294Ile
Search 100 bp 5'
Search 100 bp 3'