Canonical Allele Identifier: CA366724046
Gene: FSCN1 HGNC NCBI

Linked Data

gnomAD v4: 7-5603514-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603514T>G , CM000669.2:g.5603514T>G GRCh38
NC_000007.13:g.5643145T>G , CM000669.1:g.5643145T>G GRCh37
NC_000007.12:g.5609671T>G NCBI36
NG_030004.1:g.15710T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382361.8:c.1008T>G MANE Select ENSP00000371798.3:p.Phe336Leu
ENST00000382361.7:c.1008T>G ENSP00000371798.3:p.Phe336Leu
ENST00000405801.2:c.174T>G ENSP00000383982.2:p.Phe58Leu
ENST00000444748.5:c.174T>G ENSP00000404506.1:p.Phe58Leu
ENST00000447103.5:c.174T>G ENSP00000409967.1:p.Phe58Leu
ENST00000473330.1:n.561T>G
NM_003088.3:c.1008T>G NP_003079.1:p.Phe336Leu
NM_003088.4:c.1008T>G MANE Select NP_003079.1:p.Phe336Leu