Canonical Allele Identifier: CA366723064
Gene: FSCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603287A>C , CM000669.2:g.5603287A>C GRCh38
NC_000007.13:g.5642918A>C , CM000669.1:g.5642918A>C GRCh37
NC_000007.12:g.5609444A>C NCBI36
NG_030004.1:g.15483A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.863A>C MANE Select ENSP00000371798.3:p.Glu288Ala
ENST00000382361.7:c.863A>C ENSP00000371798.3:p.Glu288Ala
ENST00000405801.2:c.29A>C ENSP00000383982.2:p.Glu10Ala
ENST00000444748.5:c.29A>C ENSP00000404506.1:p.Glu10Ala
ENST00000447103.5:c.29A>C ENSP00000409967.1:p.Glu10Ala
ENST00000473330.1:n.416A>C
NM_003088.3:c.863A>C NP_003079.1:p.Glu288Ala
NM_003088.4:c.863A>C MANE Select NP_003079.1:p.Glu288Ala