Canonical Allele Identifier: CA366724073
Gene: FSCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603519T>A , CM000669.2:g.5603519T>A GRCh38
NC_000007.13:g.5643150T>A , CM000669.1:g.5643150T>A GRCh37
NC_000007.12:g.5609676T>A NCBI36
NG_030004.1:g.15715T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382361.8:c.1013T>A MANE Select ENSP00000371798.3:p.Ile338Asn
ENST00000382361.7:c.1013T>A ENSP00000371798.3:p.Ile338Asn
ENST00000405801.2:c.179T>A ENSP00000383982.2:p.Ile60Asn
ENST00000444748.5:c.179T>A ENSP00000404506.1:p.Ile60Asn
ENST00000447103.5:c.179T>A ENSP00000409967.1:p.Ile60Asn
ENST00000473330.1:n.566T>A
NM_003088.3:c.1013T>A NP_003079.1:p.Ile338Asn
NM_003088.4:c.1013T>A MANE Select NP_003079.1:p.Ile338Asn