Canonical Allele Identifier: CA453639877
Gene: FSCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.5642907T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603276T>C , CM000669.2:g.5603276T>C GRCh38
NC_000007.13:g.5642907T>C , CM000669.1:g.5642907T>C GRCh37
NC_000007.12:g.5609433T>C NCBI36
NG_030004.1:g.15472T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.852T>C MANE Select ENSP00000371798.3:p.Asn284=
ENST00000382361.7:c.852T>C ENSP00000371798.3:p.Asn284=
ENST00000405801.2:c.18T>C ENSP00000383982.2:p.Asn6=
ENST00000444748.5:c.18T>C ENSP00000404506.1:p.Asn6=
ENST00000447103.5:c.18T>C ENSP00000409967.1:p.Asn6=
ENST00000473330.1:n.405T>C
NM_003088.3:c.852T>C NP_003079.1:p.Asn284=
NM_003088.4:c.852T>C MANE Select NP_003079.1:p.Asn284=
Search 100 bp 5'
Search 100 bp 3'