Canonical Allele Identifier: CA578151186

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1251901695
• gnomAD v2: 7-128498657-G-A
• gnomAD v3: 7-128858603-G-A
• gnomAD v4: 7-128858603-G-A
• MyVariant Identifiers: chr7:g.128498657G>A (hg19) ; chr7:g.128858603G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128858603G>A , CM000669.2:g.128858603G>A	GRCh38
NC_000007.13:g.128498657G>A , CM000669.1:g.128498657G>A	GRCh37
NC_000007.12:g.128285893G>A	NCBI36
NG_011807.1:g.33175G>A , LRG_870:g.33175G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.*80G>A (FLNC) MANE Select	ENSP00000327145.8:n.*80G>A
ENST00000325888.12:c.*80G>A (FLNC)	ENSP00000327145.8:n.*80G>A
ENST00000346177.6:c.*80G>A (FLNC)	ENSP00000344002.6:n.*80G>A
NM_001127487.1:c.*80G>A (FLNC)	NP_001120959.1:n.*80G>A
NM_001458.4:c.*80G>A , LRG_870t1:c.*80G>A (FLNC)	NP_001449.3:n.*80G>A
NR_149055.1:n.102+3922C>T (FLNC-AS1)
NM_001127487.2:c.*80G>A (FLNC)	NP_001120959.1:n.*80G>A
NM_001458.5:c.*80G>A (FLNC) MANE Select	NP_001449.3:n.*80G>A