Canonical Allele Identifier: CA366723006

Gene: FSCN1

Linked Data

• dbSNP Id: rs1209396166
• gnomAD v3: 7-5603275-A-G
• gnomAD v4: 7-5603275-A-G
• MyVariant Identifiers: chr7:g.5642906A>G (hg19) ; chr7:g.5603275A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603275A>G , CM000669.2:g.5603275A>G	GRCh38
NC_000007.13:g.5642906A>G , CM000669.1:g.5642906A>G	GRCh37
NC_000007.12:g.5609432A>G	NCBI36
NG_030004.1:g.15471A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.851A>G MANE Select	ENSP00000371798.3:p.Asn284Ser
ENST00000382361.7:c.851A>G	ENSP00000371798.3:p.Asn284Ser
ENST00000405801.2:c.17A>G	ENSP00000383982.2:p.Asn6Ser
ENST00000444748.5:c.17A>G	ENSP00000404506.1:p.Asn6Ser
ENST00000447103.5:c.17A>G	ENSP00000409967.1:p.Asn6Ser
ENST00000473330.1:n.404A>G
NM_003088.3:c.851A>G	NP_003079.1:p.Asn284Ser
NM_003088.4:c.851A>G MANE Select	NP_003079.1:p.Asn284Ser