Canonical Allele Identifier: CA366724143
Gene: FSCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.5643170A>G (hg19) chr7:g.5603539A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603539A>G , CM000669.2:g.5603539A>G GRCh38
NC_000007.13:g.5643170A>G , CM000669.1:g.5643170A>G GRCh37
NC_000007.12:g.5609696A>G NCBI36
NG_030004.1:g.15735A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.1033A>G MANE Select ENSP00000371798.3:p.Ile345Val
ENST00000382361.7:c.1033A>G ENSP00000371798.3:p.Ile345Val
ENST00000405801.2:c.199A>G ENSP00000383982.2:p.Ile67Val
ENST00000444748.5:c.199A>G ENSP00000404506.1:p.Ile67Val
ENST00000447103.5:c.199A>G ENSP00000409967.1:p.Ile67Val
ENST00000473330.1:n.586A>G
NM_003088.3:c.1033A>G NP_003079.1:p.Ile345Val
NM_003088.4:c.1033A>G MANE Select NP_003079.1:p.Ile345Val
Search 100 bp 5'
Search 100 bp 3'