Canonical Allele Identifier: CA1685036768

Gene: FSCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603298G= , CM000669.2:g.5603298G=	GRCh38
NC_000007.13:g.5642929G= , CM000669.1:g.5642929G=	GRCh37
NC_000007.12:g.5609455G=	NCBI36
NG_030004.1:g.15494G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.874G= MANE Select	ENSP00000371798.3:p.Glu292=
ENST00000382361.7:c.874G=	ENSP00000371798.3:p.Glu292=
ENST00000405801.2:c.40G=	ENSP00000383982.2:p.Glu14=
ENST00000444748.5:c.40G=	ENSP00000404506.1:p.Glu14=
ENST00000447103.5:c.40G=	ENSP00000409967.1:p.Glu14=
ENST00000473330.1:n.427G=
NM_003088.3:c.874G=	NP_003079.1:p.Glu292=
NM_003088.4:c.874G= MANE Select	NP_003079.1:p.Glu292=