Canonical Allele Identifier: CA2557471122

Gene: FSCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603149_5603153dup , CM000669.2:g.5603149_5603153dup	GRCh38
NC_000007.13:g.5642780_5642784dup , CM000669.1:g.5642780_5642784dup	GRCh37
NC_000007.12:g.5609306_5609310dup	NCBI36
NG_030004.1:g.15345_15349dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-108_833-104dup MANE Select	ENSP00000371798.3:n.833-108_833-104dup
ENST00000382361.7:c.833-108_833-104dup	ENSP00000371798.3:n.833-108_833-104dup
ENST00000405801.2:c.-2-108_-2-104dup	ENSP00000383982.2:n.-2-108_-2-104dup
ENST00000444748.5:c.-2-108_-2-104dup	ENSP00000404506.1:n.-2-108_-2-104dup
ENST00000447103.5:c.-2-108_-2-104dup	ENSP00000409967.1:n.-2-108_-2-104dup
ENST00000473330.1:n.278_282dup
NM_003088.3:c.833-108_833-104dup	NP_003079.1:n.833-108_833-104dup
NM_003088.4:c.833-108_833-104dup MANE Select	NP_003079.1:n.833-108_833-104dup