Canonical Allele Identifier: CA839890369

Gene: FSCN1

Linked Data

• dbSNP Id: rs1234693753
• MyVariant Identifiers: chr7:g.5642794_5642805del (hg19) ; chr7:g.5603163_5603174del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603163_5603174del , CM000669.2:g.5603163_5603174del	GRCh38
NC_000007.13:g.5642794_5642805del , CM000669.1:g.5642794_5642805del	GRCh37
NC_000007.12:g.5609320_5609331del	NCBI36
NG_030004.1:g.15359_15370del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-94_833-83del MANE Select	ENSP00000371798.3:n.833-94_833-83del
ENST00000382361.7:c.833-94_833-83del	ENSP00000371798.3:n.833-94_833-83del
ENST00000405801.2:c.-2-94_-2-83del	ENSP00000383982.2:n.-2-94_-2-83del
ENST00000444748.5:c.-2-94_-2-83del	ENSP00000404506.1:n.-2-94_-2-83del
ENST00000447103.5:c.-2-94_-2-83del	ENSP00000409967.1:n.-2-94_-2-83del
ENST00000473330.1:n.292_303del
NM_003088.3:c.833-94_833-83del	NP_003079.1:n.833-94_833-83del
NM_003088.4:c.833-94_833-83del MANE Select	NP_003079.1:n.833-94_833-83del