Canonical Allele Identifier: CA366722941

Gene: FSCN1

Linked Data

• MyVariant Identifiers: chr7:g.5642890A>C (hg19) ; chr7:g.5603259A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603259A>C , CM000669.2:g.5603259A>C	GRCh38
NC_000007.13:g.5642890A>C , CM000669.1:g.5642890A>C	GRCh37
NC_000007.12:g.5609416A>C	NCBI36
NG_030004.1:g.15455A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.835A>C MANE Select	ENSP00000371798.3:p.Met279Leu
ENST00000382361.7:c.835A>C	ENSP00000371798.3:p.Met279Leu
ENST00000405801.2:c.1A>C	ENSP00000383982.2:p.Met1Leu
ENST00000444748.5:c.1A>C	ENSP00000404506.1:p.Met1Leu
ENST00000447103.5:c.1A>C	ENSP00000409967.1:p.Met1Leu
ENST00000473330.1:n.388A>C
NM_003088.3:c.835A>C	NP_003079.1:p.Met279Leu
NM_003088.4:c.835A>C MANE Select	NP_003079.1:p.Met279Leu