Canonical Allele Identifier: CA1685036692

Gene: FSCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603266T= , CM000669.2:g.5603266T=	GRCh38
NC_000007.13:g.5642897T= , CM000669.1:g.5642897T=	GRCh37
NC_000007.12:g.5609423T=	NCBI36
NG_030004.1:g.15462T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.842T= MANE Select	ENSP00000371798.3:p.Leu281=
ENST00000382361.7:c.842T=	ENSP00000371798.3:p.Leu281=
ENST00000405801.2:c.8T=	ENSP00000383982.2:p.Leu3=
ENST00000444748.5:c.8T=	ENSP00000404506.1:p.Leu3=
ENST00000447103.5:c.8T=	ENSP00000409967.1:p.Leu3=
ENST00000473330.1:n.395T=
NM_003088.3:c.842T=	NP_003079.1:p.Leu281=
NM_003088.4:c.842T= MANE Select	NP_003079.1:p.Leu281=