Canonical Allele Identifier: CA457849720

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1284934094
• gnomAD v3: 7-128854026-A-G
• gnomAD v4: 7-128854026-A-G
• MyVariant Identifiers: chr7:g.128494080A>G (hg19) ; chr7:g.128854026A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128854026A>G , CM000669.2:g.128854026A>G	GRCh38
NC_000007.13:g.128494080A>G , CM000669.1:g.128494080A>G	GRCh37
NC_000007.12:g.128281316A>G	NCBI36
NG_011807.1:g.28598A>G , LRG_870:g.28598A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6537A>G (FLNC) MANE Select	ENSP00000327145.8:p.Thr2179=
ENST00000325888.12:c.6537A>G (FLNC)	ENSP00000327145.8:p.Thr2179=
ENST00000346177.6:c.6438A>G (FLNC)	ENSP00000344002.6:p.Thr2146=
NM_001127487.1:c.6438A>G (FLNC)	NP_001120959.1:p.Thr2146=
NM_001458.4:c.6537A>G , LRG_870t1:c.6537A>G (FLNC)	NP_001449.3:p.Thr2179=
NR_149055.1:n.103-629T>C (FLNC-AS1)
NM_001127487.2:c.6438A>G (FLNC)	NP_001120959.1:p.Thr2146=
NM_001458.5:c.6537A>G (FLNC) MANE Select	NP_001449.3:p.Thr2179=