Canonical Allele Identifier: CA1685036601

Gene: FSCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603219_5603220delinsTG , CM000669.2:g.5603219_5603220delinsTG	GRCh38
NC_000007.13:g.5642850_5642851delinsTG , CM000669.1:g.5642850_5642851delinsTG	GRCh37
NC_000007.12:g.5609376_5609377delinsTG	NCBI36
NG_030004.1:g.15415_15416delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-38_833-37delinsTG MANE Select	ENSP00000371798.3:n.833-38_833-37delinsTG
ENST00000382361.7:c.833-38_833-37delinsTG	ENSP00000371798.3:n.833-38_833-37delinsTG
ENST00000405801.2:c.-2-38_-2-37delinsTG	ENSP00000383982.2:n.-2-38_-2-37delinsTG
ENST00000444748.5:c.-2-38_-2-37delinsTG	ENSP00000404506.1:n.-2-38_-2-37delinsTG
ENST00000447103.5:c.-2-38_-2-37delinsTG	ENSP00000409967.1:n.-2-38_-2-37delinsTG
ENST00000473330.1:n.348_349delinsTG
NM_003088.3:c.833-38_833-37delinsTG	NP_003079.1:n.833-38_833-37delinsTG
NM_003088.4:c.833-38_833-37delinsTG MANE Select	NP_003079.1:n.833-38_833-37delinsTG