Canonical Allele Identifier: CA578150417

Gene: FLNC

Linked Data

• dbSNP Id: rs770333344
• gnomAD v2: 7-128482805-C-CG
• gnomAD v4: 7-128842751-C-CG
• MyVariant Identifiers: chr7:g.128482806_128482807insG (hg19) ; chr7:g.128842752_128842753insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128842756dup , CM000669.2:g.128842756dup	GRCh38
NC_000007.13:g.128482810dup , CM000669.1:g.128482810dup	GRCh37
NC_000007.12:g.128270046dup	NCBI36
NG_011807.1:g.17328dup , LRG_870:g.17328dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.2390-38dup MANE Select	ENSP00000327145.8:n.2390-38dup
ENST00000325888.12:c.2390-38dup	ENSP00000327145.8:n.2390-38dup
ENST00000346177.6:c.2390-38dup	ENSP00000344002.6:n.2390-38dup
ENST00000388853.3:n.506-38dup
NM_001127487.1:c.2390-38dup	NP_001120959.1:n.2390-38dup
NM_001458.4:c.2390-38dup , LRG_870t1:c.2390-38dup	NP_001449.3:n.2390-38dup
NM_001127487.2:c.2390-38dup	NP_001120959.1:n.2390-38dup
NM_001458.5:c.2390-38dup MANE Select	NP_001449.3:n.2390-38dup