Canonical Allele Identifier: CA366722935

Gene: FSCN1

Linked Data

• MyVariant Identifiers: chr7:g.5642888G>A (hg19) ; chr7:g.5603257G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603257G>A , CM000669.2:g.5603257G>A	GRCh38
NC_000007.13:g.5642888G>A , CM000669.1:g.5642888G>A	GRCh37
NC_000007.12:g.5609414G>A	NCBI36
NG_030004.1:g.15453G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833G>A MANE Select	ENSP00000371798.3:p.Gly278Asp
ENST00000382361.7:c.833G>A	ENSP00000371798.3:p.Gly278Asp
ENST00000405801.2:c.-2G>A	ENSP00000383982.2:n.-2G>A
ENST00000444748.5:c.-2G>A	ENSP00000404506.1:n.-2G>A
ENST00000447103.5:c.-2G>A	ENSP00000409967.1:n.-2G>A
ENST00000473330.1:n.386G>A
NM_003088.3:c.833G>A	NP_003079.1:p.Gly278Asp
NM_003088.4:c.833G>A MANE Select	NP_003079.1:p.Gly278Asp