Canonical Allele Identifier: CA2580076611

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 2442810
• ClinVar RCV Id: RCV003150616
• gnomAD v4: 7-128851476-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128851479del , CM000669.2:g.128851479del	GRCh38
NC_000007.13:g.128491533del , CM000669.1:g.128491533del	GRCh37
NC_000007.12:g.128278769del	NCBI36
NG_011807.1:g.26051del , LRG_870:g.26051del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.5693del (FLNC) MANE Select	ENSP00000327145.8:p.Gly1898AlafsTer?
ENST00000325888.12:c.5693del (FLNC)	ENSP00000327145.8:p.Gly1898AlafsTer?
ENST00000346177.6:c.5594del (FLNC)	ENSP00000344002.6:p.Gly1865AlafsTer?
NM_001127487.1:c.5594del (FLNC)	NP_001120959.1:p.Gly1865AlafsTer?
NM_001458.4:c.5693del , LRG_870t1:c.5693del (FLNC)	NP_001449.3:p.Gly1898AlafsTer?
NR_149055.1:n.239del (FLNC-AS1)
NM_001127487.2:c.5594del (FLNC)	NP_001120959.1:p.Gly1865AlafsTer?
NM_001458.5:c.5693del (FLNC) MANE Select	NP_001449.3:p.Gly1898AlafsTer?