Canonical Allele Identifier: CA369220333

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1214755746
• gnomAD v2: 7-128498169-A-C
• gnomAD v4: 7-128858115-A-C
• MyVariant Identifiers: chr7:g.128498169A>C (hg19) ; chr7:g.128858115A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858115A>C , CM000669.2:g.128858115A>C	GRCh38
NC_000007.13:g.128498169A>C , CM000669.1:g.128498169A>C	GRCh37
NC_000007.12:g.128285405A>C	NCBI36
NG_011807.1:g.32687A>C , LRG_870:g.32687A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7888A>C (FLNC) MANE Select	ENSP00000327145.8:p.Lys2630Gln
ENST00000325888.12:c.7888A>C (FLNC)	ENSP00000327145.8:p.Lys2630Gln
ENST00000346177.6:c.7789A>C (FLNC)	ENSP00000344002.6:p.Lys2597Gln
NM_001127487.1:c.7789A>C (FLNC)	NP_001120959.1:p.Lys2597Gln
NM_001458.4:c.7888A>C , LRG_870t1:c.7888A>C (FLNC)	NP_001449.3:p.Lys2630Gln
NR_149055.1:n.102+4410T>G (FLNC-AS1)
NM_001127487.2:c.7789A>C (FLNC)	NP_001120959.1:p.Lys2597Gln
NM_001458.5:c.7888A>C (FLNC) MANE Select	NP_001449.3:p.Lys2630Gln