Canonical Allele Identifier: CA2681654424

Gene: FSCN1

Linked Data

• gnomAD v4: 7-5603140-GCCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603144_5603147del , CM000669.2:g.5603144_5603147del	GRCh38
NC_000007.13:g.5642775_5642778del , CM000669.1:g.5642775_5642778del	GRCh37
NC_000007.12:g.5609301_5609304del	NCBI36
NG_030004.1:g.15340_15343del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-113_833-110del MANE Select	ENSP00000371798.3:n.833-113_833-110del
ENST00000382361.7:c.833-113_833-110del	ENSP00000371798.3:n.833-113_833-110del
ENST00000405801.2:c.-2-113_-2-110del	ENSP00000383982.2:n.-2-113_-2-110del
ENST00000444748.5:c.-2-113_-2-110del	ENSP00000404506.1:n.-2-113_-2-110del
ENST00000447103.5:c.-2-113_-2-110del	ENSP00000409967.1:n.-2-113_-2-110del
ENST00000473330.1:n.273_276del
NM_003088.3:c.833-113_833-110del	NP_003079.1:n.833-113_833-110del
NM_003088.4:c.833-113_833-110del MANE Select	NP_003079.1:n.833-113_833-110del