Canonical Allele Identifier: CA1685036819

Gene: FSCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603322C= , CM000669.2:g.5603322C=	GRCh38
NC_000007.13:g.5642953C= , CM000669.1:g.5642953C=	GRCh37
NC_000007.12:g.5609479C=	NCBI36
NG_030004.1:g.15518C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.898C= MANE Select	ENSP00000371798.3:p.Arg300=
ENST00000382361.7:c.898C=	ENSP00000371798.3:p.Arg300=
ENST00000405801.2:c.64C=	ENSP00000383982.2:p.Arg22=
ENST00000444748.5:c.64C=	ENSP00000404506.1:p.Arg22=
ENST00000447103.5:c.64C=	ENSP00000409967.1:p.Arg22=
ENST00000473330.1:n.451C=
NM_003088.3:c.898C=	NP_003079.1:p.Arg300=
NM_003088.4:c.898C= MANE Select	NP_003079.1:p.Arg300=