Canonical Allele Identifier: CA1685037213
Gene: FSCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603521G= , CM000669.2:g.5603521G= GRCh38
NC_000007.13:g.5643152G= , CM000669.1:g.5643152G= GRCh37
NC_000007.12:g.5609678G= NCBI36
NG_030004.1:g.15717G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382361.8:c.1015G= MANE Select ENSP00000371798.3:p.Glu339=
ENST00000382361.7:c.1015G= ENSP00000371798.3:p.Glu339=
ENST00000405801.2:c.181G= ENSP00000383982.2:p.Glu61=
ENST00000444748.5:c.181G= ENSP00000404506.1:p.Glu61=
ENST00000447103.5:c.181G= ENSP00000409967.1:p.Glu61=
ENST00000473330.1:n.568G=
NM_003088.3:c.1015G= NP_003079.1:p.Glu339=
NM_003088.4:c.1015G= MANE Select NP_003079.1:p.Glu339=