Canonical Allele Identifier: CA366723142

Gene: FSCN1

Linked Data

• MyVariant Identifiers: chr7:g.5642931G>T (hg19) ; chr7:g.5603300G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603300G>T , CM000669.2:g.5603300G>T	GRCh38
NC_000007.13:g.5642931G>T , CM000669.1:g.5642931G>T	GRCh37
NC_000007.12:g.5609457G>T	NCBI36
NG_030004.1:g.15496G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.876G>T MANE Select	ENSP00000371798.3:p.Glu292Asp
ENST00000382361.7:c.876G>T	ENSP00000371798.3:p.Glu292Asp
ENST00000405801.2:c.42G>T	ENSP00000383982.2:p.Glu14Asp
ENST00000444748.5:c.42G>T	ENSP00000404506.1:p.Glu14Asp
ENST00000447103.5:c.42G>T	ENSP00000409967.1:p.Glu14Asp
ENST00000473330.1:n.429G>T
NM_003088.3:c.876G>T	NP_003079.1:p.Glu292Asp
NM_003088.4:c.876G>T MANE Select	NP_003079.1:p.Glu292Asp