Canonical Allele Identifier: CA369211634

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1233340289
• gnomAD v3: 7-128853011-T-C
• gnomAD v4: 7-128853011-T-C
• MyVariant Identifiers: chr7:g.128493065T>C (hg19) ; chr7:g.128853011T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128853011T>C , CM000669.2:g.128853011T>C	GRCh38
NC_000007.13:g.128493065T>C , CM000669.1:g.128493065T>C	GRCh37
NC_000007.12:g.128280301T>C	NCBI36
NG_011807.1:g.27583T>C , LRG_870:g.27583T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6188T>C (FLNC) MANE Select	ENSP00000327145.8:p.Ile2063Thr
ENST00000325888.12:c.6188T>C (FLNC)	ENSP00000327145.8:p.Ile2063Thr
ENST00000346177.6:c.6089T>C (FLNC)	ENSP00000344002.6:p.Ile2030Thr
NM_001127487.1:c.6089T>C (FLNC)	NP_001120959.1:p.Ile2030Thr
NM_001458.4:c.6188T>C , LRG_870t1:c.6188T>C (FLNC)	NP_001449.3:p.Ile2063Thr
NR_149055.1:n.215+274A>G (FLNC-AS1)
NM_001127487.2:c.6089T>C (FLNC)	NP_001120959.1:p.Ile2030Thr
NM_001458.5:c.6188T>C (FLNC) MANE Select	NP_001449.3:p.Ile2063Thr