Canonical Allele Identifier: CA578150596

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1344074158
• gnomAD v2: 7-128492828-G-A
• gnomAD v4: 7-128852774-G-A
• MyVariant Identifiers: chr7:g.128492828G>A (hg19) ; chr7:g.128852774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128852774G>A , CM000669.2:g.128852774G>A	GRCh38
NC_000007.13:g.128492828G>A , CM000669.1:g.128492828G>A	GRCh37
NC_000007.12:g.128280064G>A	NCBI36
NG_011807.1:g.27346G>A , LRG_870:g.27346G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6004+22G>A (FLNC) MANE Select	ENSP00000327145.8:n.6004+22G>A
ENST00000325888.12:c.6004+22G>A (FLNC)	ENSP00000327145.8:n.6004+22G>A
ENST00000346177.6:c.5905+22G>A (FLNC)	ENSP00000344002.6:n.5905+22G>A
NM_001127487.1:c.5905+22G>A (FLNC)	NP_001120959.1:n.5905+22G>A
NM_001458.4:c.6004+22G>A , LRG_870t1:c.6004+22G>A (FLNC)	NP_001449.3:n.6004+22G>A
NR_149055.1:n.215+511C>T (FLNC-AS1)
NM_001127487.2:c.5905+22G>A (FLNC)	NP_001120959.1:n.5905+22G>A
NM_001458.5:c.6004+22G>A (FLNC) MANE Select	NP_001449.3:n.6004+22G>A