Canonical Allele Identifier: CA2713518520

Gene: FSCN1

Linked Data

• dbSNP Id: rs1191368691

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603195A>G , CM000669.2:g.5603195A>G	GRCh38
NC_000007.13:g.5642826A>G , CM000669.1:g.5642826A>G	GRCh37
NC_000007.12:g.5609352A>G	NCBI36
NG_030004.1:g.15391A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-62A>G MANE Select	ENSP00000371798.3:n.833-62A>G
ENST00000382361.7:c.833-62A>G	ENSP00000371798.3:n.833-62A>G
ENST00000405801.2:c.-2-62A>G	ENSP00000383982.2:n.-2-62A>G
ENST00000444748.5:c.-2-62A>G	ENSP00000404506.1:n.-2-62A>G
ENST00000447103.5:c.-2-62A>G	ENSP00000409967.1:n.-2-62A>G
ENST00000473330.1:n.324A>G
NM_003088.3:c.833-62A>G	NP_003079.1:n.833-62A>G
NM_003088.4:c.833-62A>G MANE Select	NP_003079.1:n.833-62A>G