Canonical Allele Identifier: CA839890363

Gene: FSCN1

Linked Data

• dbSNP Id: rs1348321217
• gnomAD v3: 7-5603155-T-TGC
• gnomAD v4: 7-5603155-T-TGC
• MyVariant Identifiers: chr7:g.5642786_5642787insGC (hg19) ; chr7:g.5603155_5603156insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5603156_5603157insCG , CM000669.2:g.5603156_5603157insCG	GRCh38
NC_000007.13:g.5642787_5642788insCG , CM000669.1:g.5642787_5642788insCG	GRCh37
NC_000007.12:g.5609313_5609314insCG	NCBI36
NG_030004.1:g.15352_15353insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382361.8:c.833-101_833-100insCG MANE Select	ENSP00000371798.3:n.833-101_833-100insCG
ENST00000382361.7:c.833-101_833-100insCG	ENSP00000371798.3:n.833-101_833-100insCG
ENST00000405801.2:c.-2-101_-2-100insCG	ENSP00000383982.2:n.-2-101_-2-100insCG
ENST00000444748.5:c.-2-101_-2-100insCG	ENSP00000404506.1:n.-2-101_-2-100insCG
ENST00000447103.5:c.-2-101_-2-100insCG	ENSP00000409967.1:n.-2-101_-2-100insCG
ENST00000473330.1:n.285_286insCG
NM_003088.3:c.833-101_833-100insCG	NP_003079.1:n.833-101_833-100insCG
NM_003088.4:c.833-101_833-100insCG MANE Select	NP_003079.1:n.833-101_833-100insCG