Canonical Allele Identifier: CA2681654449

Gene: FSCN1

Linked Data

• gnomAD v4: 7-5603162-ACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603163_5603165del , CM000669.2:g.5603163_5603165del	GRCh38
NC_000007.13:g.5642794_5642796del , CM000669.1:g.5642794_5642796del	GRCh37
NC_000007.12:g.5609320_5609322del	NCBI36
NG_030004.1:g.15359_15361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-94_833-92del MANE Select	ENSP00000371798.3:n.833-94_833-92del
ENST00000382361.7:c.833-94_833-92del	ENSP00000371798.3:n.833-94_833-92del
ENST00000405801.2:c.-2-94_-2-92del	ENSP00000383982.2:n.-2-94_-2-92del
ENST00000444748.5:c.-2-94_-2-92del	ENSP00000404506.1:n.-2-94_-2-92del
ENST00000447103.5:c.-2-94_-2-92del	ENSP00000409967.1:n.-2-94_-2-92del
ENST00000473330.1:n.292_294del
NM_003088.3:c.833-94_833-92del	NP_003079.1:n.833-94_833-92del
NM_003088.4:c.833-94_833-92del MANE Select	NP_003079.1:n.833-94_833-92del