Canonical Allele Identifier: CA1685037243
Gene: FSCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603534G= , CM000669.2:g.5603534G= GRCh38
NC_000007.13:g.5643165G= , CM000669.1:g.5643165G= GRCh37
NC_000007.12:g.5609691G= NCBI36
NG_030004.1:g.15730G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.1028G= MANE Select ENSP00000371798.3:p.Arg343=
ENST00000382361.7:c.1028G= ENSP00000371798.3:p.Arg343=
ENST00000405801.2:c.194G= ENSP00000383982.2:p.Arg65=
ENST00000444748.5:c.194G= ENSP00000404506.1:p.Arg65=
ENST00000447103.5:c.194G= ENSP00000409967.1:p.Arg65=
ENST00000473330.1:n.581G=
NM_003088.3:c.1028G= NP_003079.1:p.Arg343=
NM_003088.4:c.1028G= MANE Select NP_003079.1:p.Arg343=