Canonical Allele Identifier: CA457592149

Gene: FLNC FLNC-AS1

Linked Data

• gnomAD v4: 7-128858460-C-A
• COSMIC: COSM1085389
• MyVariant Identifiers: chr7:g.128498514C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858460C>A , CM000669.2:g.128858460C>A	GRCh38
NC_000007.13:g.128498514C>A , CM000669.1:g.128498514C>A	GRCh37
NC_000007.12:g.128285750C>A	NCBI36
NG_011807.1:g.33032C>A , LRG_870:g.33032C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.8115C>A (FLNC) MANE Select	ENSP00000327145.8:p.Ile2705=
ENST00000325888.12:c.8115C>A (FLNC)	ENSP00000327145.8:p.Ile2705=
ENST00000346177.6:c.8016C>A (FLNC)	ENSP00000344002.6:p.Ile2672=
NM_001127487.1:c.8016C>A (FLNC)	NP_001120959.1:p.Ile2672=
NM_001458.4:c.8115C>A , LRG_870t1:c.8115C>A (FLNC)	NP_001449.3:p.Ile2705=
NR_149055.1:n.102+4065G>T (FLNC-AS1)
NM_001127487.2:c.8016C>A (FLNC)	NP_001120959.1:p.Ile2672=
NM_001458.5:c.8115C>A (FLNC) MANE Select	NP_001449.3:p.Ile2705=