Canonical Allele Identifier: CA366722972
Gene: FSCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.5642896C>A (hg19) chr7:g.5603265C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603265C>A , CM000669.2:g.5603265C>A GRCh38
NC_000007.13:g.5642896C>A , CM000669.1:g.5642896C>A GRCh37
NC_000007.12:g.5609422C>A NCBI36
NG_030004.1:g.15461C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.841C>A MANE Select ENSP00000371798.3:p.Leu281Met
ENST00000382361.7:c.841C>A ENSP00000371798.3:p.Leu281Met
ENST00000405801.2:c.7C>A ENSP00000383982.2:p.Leu3Met
ENST00000444748.5:c.7C>A ENSP00000404506.1:p.Leu3Met
ENST00000447103.5:c.7C>A ENSP00000409967.1:p.Leu3Met
ENST00000473330.1:n.394C>A
NM_003088.3:c.841C>A NP_003079.1:p.Leu281Met
NM_003088.4:c.841C>A MANE Select NP_003079.1:p.Leu281Met
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