Canonical Allele Identifier: CA1685036433
Gene: FSCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1584303779
gnomAD v4: 7-5603121-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603121C>T , CM000669.2:g.5603121C>T GRCh38
NC_000007.13:g.5642752C>T , CM000669.1:g.5642752C>T GRCh37
NC_000007.12:g.5609278C>T NCBI36
NG_030004.1:g.15317C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.833-136C>T MANE Select ENSP00000371798.3:n.833-136C>T
ENST00000382361.7:c.833-136C>T ENSP00000371798.3:n.833-136C>T
ENST00000405801.2:c.-2-136C>T ENSP00000383982.2:n.-2-136C>T
ENST00000444748.5:c.-2-136C>T ENSP00000404506.1:n.-2-136C>T
ENST00000447103.5:c.-2-136C>T ENSP00000409967.1:n.-2-136C>T
ENST00000473330.1:n.250C>T
NM_003088.3:c.833-136C>T NP_003079.1:n.833-136C>T
NM_003088.4:c.833-136C>T MANE Select NP_003079.1:n.833-136C>T
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