Canonical Allele Identifier: CA2681654456
Gene: FSCN1 HGNC NCBI

Linked Data

gnomAD v4: 7-5603169-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603169G>T , CM000669.2:g.5603169G>T GRCh38
NC_000007.13:g.5642800G>T , CM000669.1:g.5642800G>T GRCh37
NC_000007.12:g.5609326G>T NCBI36
NG_030004.1:g.15365G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.833-88G>T MANE Select ENSP00000371798.3:n.833-88G>T
ENST00000382361.7:c.833-88G>T ENSP00000371798.3:n.833-88G>T
ENST00000405801.2:c.-2-88G>T ENSP00000383982.2:n.-2-88G>T
ENST00000444748.5:c.-2-88G>T ENSP00000404506.1:n.-2-88G>T
ENST00000447103.5:c.-2-88G>T ENSP00000409967.1:n.-2-88G>T
ENST00000473330.1:n.298G>T
NM_003088.3:c.833-88G>T NP_003079.1:n.833-88G>T
NM_003088.4:c.833-88G>T MANE Select NP_003079.1:n.833-88G>T
Search 100 bp 5'
Search 100 bp 3'