Canonical Allele Identifier: CA4147459
Gene: FSCN1 HGNC NCBI

Linked Data

dbSNP Id: rs746374083
gnomAD v2: 7-5642967-G-T
gnomAD v3: 7-5603336-G-T
gnomAD v4: 7-5603336-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603336G>T , CM000669.2:g.5603336G>T GRCh38
NC_000007.13:g.5642967G>T , CM000669.1:g.5642967G>T GRCh37
NC_000007.12:g.5609493G>T NCBI36
NG_030004.1:g.15532G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.912G>T MANE Select ENSP00000371798.3:p.Lys304Asn
ENST00000382361.7:c.912G>T ENSP00000371798.3:p.Lys304Asn
ENST00000405801.2:c.78G>T ENSP00000383982.2:p.Lys26Asn
ENST00000444748.5:c.78G>T ENSP00000404506.1:p.Lys26Asn
ENST00000447103.5:c.78G>T ENSP00000409967.1:p.Lys26Asn
ENST00000473330.1:n.465G>T
NM_003088.3:c.912G>T NP_003079.1:p.Lys304Asn
NM_003088.4:c.912G>T MANE Select NP_003079.1:p.Lys304Asn