Canonical Allele Identifier: CA457847838

Gene: FLNC

Linked Data

• ClinVar Variation Id: 2175652
• ClinVar RCV Id: RCV002579391
• gnomAD v4: 7-128842864-C-T
• MyVariant Identifiers: chr7:g.128482918C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128842864C>T , CM000669.2:g.128842864C>T	GRCh38
NC_000007.13:g.128482918C>T , CM000669.1:g.128482918C>T	GRCh37
NC_000007.12:g.128270154C>T	NCBI36
NG_011807.1:g.17436C>T , LRG_870:g.17436C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.2460C>T MANE Select	ENSP00000327145.8:p.Asp820=
ENST00000325888.12:c.2460C>T	ENSP00000327145.8:p.Asp820=
ENST00000346177.6:c.2460C>T	ENSP00000344002.6:p.Asp820=
NM_001127487.1:c.2460C>T	NP_001120959.1:p.Asp820=
NM_001458.4:c.2460C>T , LRG_870t1:c.2460C>T	NP_001449.3:p.Asp820=
NM_001127487.2:c.2460C>T	NP_001120959.1:p.Asp820=
NM_001458.5:c.2460C>T MANE Select	NP_001449.3:p.Asp820=