Canonical Allele Identifier: CA1685036487
Gene: FSCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603153C= , CM000669.2:g.5603153C= GRCh38
NC_000007.13:g.5642784C= , CM000669.1:g.5642784C= GRCh37
NC_000007.12:g.5609310C= NCBI36
NG_030004.1:g.15349C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.833-104C= MANE Select ENSP00000371798.3:n.833-104C=
ENST00000382361.7:c.833-104C= ENSP00000371798.3:n.833-104C=
ENST00000405801.2:c.-2-104C= ENSP00000383982.2:n.-2-104C=
ENST00000444748.5:c.-2-104C= ENSP00000404506.1:n.-2-104C=
ENST00000447103.5:c.-2-104C= ENSP00000409967.1:n.-2-104C=
ENST00000473330.1:n.282C=
NM_003088.3:c.833-104C= NP_003079.1:n.833-104C=
NM_003088.4:c.833-104C= MANE Select NP_003079.1:n.833-104C=
Search 100 bp 5'
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