Canonical Allele Identifier: CA369221303

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1234441171
• gnomAD v2: 7-128498435-G-A
• gnomAD v4: 7-128858381-G-A
• MyVariant Identifiers: chr7:g.128498435G>A (hg19) ; chr7:g.128858381G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858381G>A , CM000669.2:g.128858381G>A	GRCh38
NC_000007.13:g.128498435G>A , CM000669.1:g.128498435G>A	GRCh37
NC_000007.12:g.128285671G>A	NCBI36
NG_011807.1:g.32953G>A , LRG_870:g.32953G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.8036G>A (FLNC) MANE Select	ENSP00000327145.8:p.Cys2679Tyr
ENST00000325888.12:c.8036G>A (FLNC)	ENSP00000327145.8:p.Cys2679Tyr
ENST00000346177.6:c.7937G>A (FLNC)	ENSP00000344002.6:p.Cys2646Tyr
NM_001127487.1:c.7937G>A (FLNC)	NP_001120959.1:p.Cys2646Tyr
NM_001458.4:c.8036G>A , LRG_870t1:c.8036G>A (FLNC)	NP_001449.3:p.Cys2679Tyr
NR_149055.1:n.102+4144C>T (FLNC-AS1)
NM_001127487.2:c.7937G>A (FLNC)	NP_001120959.1:p.Cys2646Tyr
NM_001458.5:c.8036G>A (FLNC) MANE Select	NP_001449.3:p.Cys2679Tyr