Canonical Allele Identifier: CA1685036449

Gene: FSCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603131_5603132delinsGA , CM000669.2:g.5603131_5603132delinsGA	GRCh38
NC_000007.13:g.5642762_5642763delinsGA , CM000669.1:g.5642762_5642763delinsGA	GRCh37
NC_000007.12:g.5609288_5609289delinsGA	NCBI36
NG_030004.1:g.15327_15328delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-126_833-125delinsGA MANE Select	ENSP00000371798.3:n.833-126_833-125delinsGA
ENST00000382361.7:c.833-126_833-125delinsGA	ENSP00000371798.3:n.833-126_833-125delinsGA
ENST00000405801.2:c.-2-126_-2-125delinsGA	ENSP00000383982.2:n.-2-126_-2-125delinsGA
ENST00000444748.5:c.-2-126_-2-125delinsGA	ENSP00000404506.1:n.-2-126_-2-125delinsGA
ENST00000447103.5:c.-2-126_-2-125delinsGA	ENSP00000409967.1:n.-2-126_-2-125delinsGA
ENST00000473330.1:n.260_261delinsGA
NM_003088.3:c.833-126_833-125delinsGA	NP_003079.1:n.833-126_833-125delinsGA
NM_003088.4:c.833-126_833-125delinsGA MANE Select	NP_003079.1:n.833-126_833-125delinsGA