Canonical Allele Identifier: CA366723466
Gene: FSCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603340G>T , CM000669.2:g.5603340G>T GRCh38
NC_000007.13:g.5642971G>T , CM000669.1:g.5642971G>T GRCh37
NC_000007.12:g.5609497G>T NCBI36
NG_030004.1:g.15536G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.916G>T MANE Select ENSP00000371798.3:p.Ala306Ser
ENST00000382361.7:c.916G>T ENSP00000371798.3:p.Ala306Ser
ENST00000405801.2:c.82G>T ENSP00000383982.2:p.Ala28Ser
ENST00000444748.5:c.82G>T ENSP00000404506.1:p.Ala28Ser
ENST00000447103.5:c.82G>T ENSP00000409967.1:p.Ala28Ser
ENST00000473330.1:n.469G>T
NM_003088.3:c.916G>T NP_003079.1:p.Ala306Ser
NM_003088.4:c.916G>T MANE Select NP_003079.1:p.Ala306Ser