Canonical Allele Identifier: CA2681654464

Gene: FSCN1

Linked Data

• gnomAD v4: 7-5603174-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603174_5603175insG , CM000669.2:g.5603174_5603175insG	GRCh38
NC_000007.13:g.5642805_5642806insG , CM000669.1:g.5642805_5642806insG	GRCh37
NC_000007.12:g.5609331_5609332insG	NCBI36
NG_030004.1:g.15370_15371insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-83_833-82insG MANE Select	ENSP00000371798.3:n.833-83_833-82insG
ENST00000382361.7:c.833-83_833-82insG	ENSP00000371798.3:n.833-83_833-82insG
ENST00000405801.2:c.-2-83_-2-82insG	ENSP00000383982.2:n.-2-83_-2-82insG
ENST00000444748.5:c.-2-83_-2-82insG	ENSP00000404506.1:n.-2-83_-2-82insG
ENST00000447103.5:c.-2-83_-2-82insG	ENSP00000409967.1:n.-2-83_-2-82insG
ENST00000473330.1:n.303_304insG
NM_003088.3:c.833-83_833-82insG	NP_003079.1:n.833-83_833-82insG
NM_003088.4:c.833-83_833-82insG MANE Select	NP_003079.1:n.833-83_833-82insG