Canonical Allele Identifier: CA153233240

Gene: FSCN1

Linked Data

• dbSNP Id: rs1037224897
• gnomAD v4: 7-5603175-A-T
• MyVariant Identifiers: chr7:g.5642806A>T (hg19) ; chr7:g.5603175A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603175A>T , CM000669.2:g.5603175A>T	GRCh38
NC_000007.13:g.5642806A>T , CM000669.1:g.5642806A>T	GRCh37
NC_000007.12:g.5609332A>T	NCBI36
NG_030004.1:g.15371A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-82A>T MANE Select	ENSP00000371798.3:n.833-82A>T
ENST00000382361.7:c.833-82A>T	ENSP00000371798.3:n.833-82A>T
ENST00000405801.2:c.-2-82A>T	ENSP00000383982.2:n.-2-82A>T
ENST00000444748.5:c.-2-82A>T	ENSP00000404506.1:n.-2-82A>T
ENST00000447103.5:c.-2-82A>T	ENSP00000409967.1:n.-2-82A>T
ENST00000473330.1:n.304A>T
NM_003088.3:c.833-82A>T	NP_003079.1:n.833-82A>T
NM_003088.4:c.833-82A>T MANE Select	NP_003079.1:n.833-82A>T