Canonical Allele Identifier: CA1685036578
Gene: FSCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603212G= , CM000669.2:g.5603212G= GRCh38
NC_000007.13:g.5642843G= , CM000669.1:g.5642843G= GRCh37
NC_000007.12:g.5609369G= NCBI36
NG_030004.1:g.15408G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.833-45G= MANE Select ENSP00000371798.3:n.833-45G=
ENST00000382361.7:c.833-45G= ENSP00000371798.3:n.833-45G=
ENST00000405801.2:c.-2-45G= ENSP00000383982.2:n.-2-45G=
ENST00000444748.5:c.-2-45G= ENSP00000404506.1:n.-2-45G=
ENST00000447103.5:c.-2-45G= ENSP00000409967.1:n.-2-45G=
ENST00000473330.1:n.341G=
NM_003088.3:c.833-45G= NP_003079.1:n.833-45G=
NM_003088.4:c.833-45G= MANE Select NP_003079.1:n.833-45G=
Search 100 bp 5'
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