Canonical Allele Identifier: CA1685036678

Gene: FSCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603258T= , CM000669.2:g.5603258T=	GRCh38
NC_000007.13:g.5642889T= , CM000669.1:g.5642889T=	GRCh37
NC_000007.12:g.5609415T=	NCBI36
NG_030004.1:g.15454T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.834T= MANE Select	ENSP00000371798.3:p.Gly278=
ENST00000382361.7:c.834T=	ENSP00000371798.3:p.Gly278=
ENST00000405801.2:c.-1T=	ENSP00000383982.2:n.-1T=
ENST00000444748.5:c.-1T=	ENSP00000404506.1:n.-1T=
ENST00000447103.5:c.-1T=	ENSP00000409967.1:n.-1T=
ENST00000473330.1:n.387T=
NM_003088.3:c.834T=	NP_003079.1:p.Gly278=
NM_003088.4:c.834T= MANE Select	NP_003079.1:p.Gly278=