Canonical Allele Identifier: CA4476087

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 1157454
• ClinVar RCV Id: RCV001500501 ; RCV001581161 ; RCV003365417
• dbSNP Id: rs767691386
• ExAC: 7:128494513 G / A
• gnomAD v2: 7-128494513-G-A
• gnomAD v3: 7-128854459-G-A
• gnomAD v4: 7-128854459-G-A
• MyVariant Identifiers: chr7:g.128494513G>A (hg19) ; chr7:g.128854459G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128854459G>A , CM000669.2:g.128854459G>A	GRCh38
NC_000007.13:g.128494513G>A , CM000669.1:g.128494513G>A	GRCh37
NC_000007.12:g.128281749G>A	NCBI36
NG_011807.1:g.29031G>A , LRG_870:g.29031G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.6774G>A (FLNC) MANE Select	ENSP00000327145.8:p.Ser2258=
ENST00000325888.12:c.6774G>A (FLNC)	ENSP00000327145.8:p.Ser2258=
ENST00000346177.6:c.6675G>A (FLNC)	ENSP00000344002.6:p.Ser2225=
NM_001127487.1:c.6675G>A (FLNC)	NP_001120959.1:p.Ser2225=
NM_001458.4:c.6774G>A , LRG_870t1:c.6774G>A (FLNC)	NP_001449.3:p.Ser2258=
NR_149055.1:n.103-1062C>T (FLNC-AS1)
NM_001127487.2:c.6675G>A (FLNC)	NP_001120959.1:p.Ser2225=
NM_001458.5:c.6774G>A (FLNC) MANE Select	NP_001449.3:p.Ser2258=