Canonical Allele Identifier: CA2681654529
Gene: FSCN1 HGNC NCBI

Linked Data

gnomAD v4: 7-5603451-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603451C>G , CM000669.2:g.5603451C>G GRCh38
NC_000007.13:g.5643082C>G , CM000669.1:g.5643082C>G GRCh37
NC_000007.12:g.5609608C>G NCBI36
NG_030004.1:g.15647C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382361.8:c.989+38C>G MANE Select ENSP00000371798.3:n.989+38C>G
ENST00000382361.7:c.989+38C>G ENSP00000371798.3:n.989+38C>G
ENST00000405801.2:c.155+38C>G ENSP00000383982.2:n.155+38C>G
ENST00000444748.5:c.155+38C>G ENSP00000404506.1:n.155+38C>G
ENST00000447103.5:c.155+38C>G ENSP00000409967.1:n.155+38C>G
ENST00000473330.1:n.542+38C>G
NM_003088.3:c.989+38C>G NP_003079.1:n.989+38C>G
NM_003088.4:c.989+38C>G MANE Select NP_003079.1:n.989+38C>G
Search 100 bp 5'
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