Canonical Allele Identifier: CA366723322
Gene: FSCN1 HGNC NCBI

Linked Data

gnomAD v4: 7-5603319-G-T
MyVariant Identifiers: chr7:g.5642950G>T (hg19) chr7:g.5603319G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603319G>T , CM000669.2:g.5603319G>T GRCh38
NC_000007.13:g.5642950G>T , CM000669.1:g.5642950G>T GRCh37
NC_000007.12:g.5609476G>T NCBI36
NG_030004.1:g.15515G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.895G>T MANE Select ENSP00000371798.3:p.Asp299Tyr
ENST00000382361.7:c.895G>T ENSP00000371798.3:p.Asp299Tyr
ENST00000405801.2:c.61G>T ENSP00000383982.2:p.Asp21Tyr
ENST00000444748.5:c.61G>T ENSP00000404506.1:p.Asp21Tyr
ENST00000447103.5:c.61G>T ENSP00000409967.1:p.Asp21Tyr
ENST00000473330.1:n.448G>T
NM_003088.3:c.895G>T NP_003079.1:p.Asp299Tyr
NM_003088.4:c.895G>T MANE Select NP_003079.1:p.Asp299Tyr
Search 100 bp 5'
Search 100 bp 3'