Canonical Allele Identifier: CA1685036516

Gene: FSCN1

Linked Data

• dbSNP Id: rs1785864624

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603171G>C , CM000669.2:g.5603171G>C	GRCh38
NC_000007.13:g.5642802G>C , CM000669.1:g.5642802G>C	GRCh37
NC_000007.12:g.5609328G>C	NCBI36
NG_030004.1:g.15367G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-86G>C MANE Select	ENSP00000371798.3:n.833-86G>C
ENST00000382361.7:c.833-86G>C	ENSP00000371798.3:n.833-86G>C
ENST00000405801.2:c.-2-86G>C	ENSP00000383982.2:n.-2-86G>C
ENST00000444748.5:c.-2-86G>C	ENSP00000404506.1:n.-2-86G>C
ENST00000447103.5:c.-2-86G>C	ENSP00000409967.1:n.-2-86G>C
ENST00000473330.1:n.300G>C
NM_003088.3:c.833-86G>C	NP_003079.1:n.833-86G>C
NM_003088.4:c.833-86G>C MANE Select	NP_003079.1:n.833-86G>C