Canonical Allele Identifier: CA1685037038
Gene: FSCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603445C= , CM000669.2:g.5603445C= GRCh38
NC_000007.13:g.5643076C= , CM000669.1:g.5643076C= GRCh37
NC_000007.12:g.5609602C= NCBI36
NG_030004.1:g.15641C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382361.8:c.989+32C= MANE Select ENSP00000371798.3:n.989+32C=
ENST00000382361.7:c.989+32C= ENSP00000371798.3:n.989+32C=
ENST00000405801.2:c.155+32C= ENSP00000383982.2:n.155+32C=
ENST00000444748.5:c.155+32C= ENSP00000404506.1:n.155+32C=
ENST00000447103.5:c.155+32C= ENSP00000409967.1:n.155+32C=
ENST00000473330.1:n.542+32C=
NM_003088.3:c.989+32C= NP_003079.1:n.989+32C=
NM_003088.4:c.989+32C= MANE Select NP_003079.1:n.989+32C=
Search 100 bp 5'
Search 100 bp 3'