Canonical Allele Identifier: CA1685036575

Gene: FSCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603210_5603211delinsTA , CM000669.2:g.5603210_5603211delinsTA	GRCh38
NC_000007.13:g.5642841_5642842delinsTA , CM000669.1:g.5642841_5642842delinsTA	GRCh37
NC_000007.12:g.5609367_5609368delinsTA	NCBI36
NG_030004.1:g.15406_15407delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-47_833-46delinsTA MANE Select	ENSP00000371798.3:n.833-47_833-46delinsTA
ENST00000382361.7:c.833-47_833-46delinsTA	ENSP00000371798.3:n.833-47_833-46delinsTA
ENST00000405801.2:c.-2-47_-2-46delinsTA	ENSP00000383982.2:n.-2-47_-2-46delinsTA
ENST00000444748.5:c.-2-47_-2-46delinsTA	ENSP00000404506.1:n.-2-47_-2-46delinsTA
ENST00000447103.5:c.-2-47_-2-46delinsTA	ENSP00000409967.1:n.-2-47_-2-46delinsTA
ENST00000473330.1:n.339_340delinsTA
NM_003088.3:c.833-47_833-46delinsTA	NP_003079.1:n.833-47_833-46delinsTA
NM_003088.4:c.833-47_833-46delinsTA MANE Select	NP_003079.1:n.833-47_833-46delinsTA