Canonical Allele Identifier: CA1685036538

Gene: FSCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603181_5603186delinsGTGAGC , CM000669.2:g.5603181_5603186delinsGTGAGC	GRCh38
NC_000007.13:g.5642812_5642817delinsGTGAGC , CM000669.1:g.5642812_5642817delinsGTGAGC	GRCh37
NC_000007.12:g.5609338_5609343delinsGTGAGC	NCBI36
NG_030004.1:g.15377_15382delinsGTGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-76_833-71delinsGTGAGC MANE Select	ENSP00000371798.3:n.833-76_833-71delinsGTGAGC
ENST00000382361.7:c.833-76_833-71delinsGTGAGC	ENSP00000371798.3:n.833-76_833-71delinsGTGAGC
ENST00000405801.2:c.-2-76_-2-71delinsGTGAGC	ENSP00000383982.2:n.-2-76_-2-71delinsGTGAGC
ENST00000444748.5:c.-2-76_-2-71delinsGTGAGC	ENSP00000404506.1:n.-2-76_-2-71delinsGTGAGC
ENST00000447103.5:c.-2-76_-2-71delinsGTGAGC	ENSP00000409967.1:n.-2-76_-2-71delinsGTGAGC
ENST00000473330.1:n.310_315delinsGTGAGC
NM_003088.3:c.833-76_833-71delinsGTGAGC	NP_003079.1:n.833-76_833-71delinsGTGAGC
NM_003088.4:c.833-76_833-71delinsGTGAGC MANE Select	NP_003079.1:n.833-76_833-71delinsGTGAGC