Canonical Allele Identifier: CA1685036542

Gene: FSCN1

Linked Data

• dbSNP Id: rs1785864883

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603183_5603187del , CM000669.2:g.5603183_5603187del	GRCh38
NC_000007.13:g.5642814_5642818del , CM000669.1:g.5642814_5642818del	GRCh37
NC_000007.12:g.5609340_5609344del	NCBI36
NG_030004.1:g.15379_15383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-74_833-70del MANE Select	ENSP00000371798.3:n.833-74_833-70del
ENST00000382361.7:c.833-74_833-70del	ENSP00000371798.3:n.833-74_833-70del
ENST00000405801.2:c.-2-74_-2-70del	ENSP00000383982.2:n.-2-74_-2-70del
ENST00000444748.5:c.-2-74_-2-70del	ENSP00000404506.1:n.-2-74_-2-70del
ENST00000447103.5:c.-2-74_-2-70del	ENSP00000409967.1:n.-2-74_-2-70del
ENST00000473330.1:n.312_316del
NM_003088.3:c.833-74_833-70del	NP_003079.1:n.833-74_833-70del
NM_003088.4:c.833-74_833-70del MANE Select	NP_003079.1:n.833-74_833-70del