Canonical Allele Identifier: CA369217072

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 1384880
• ClinVar RCV Id: RCV001902676
• dbSNP Id: rs2128940164
• MyVariant Identifiers: chr7:g.128496699A>G (hg19) ; chr7:g.128856645A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128856645A>G , CM000669.2:g.128856645A>G	GRCh38
NC_000007.13:g.128496699A>G , CM000669.1:g.128496699A>G	GRCh37
NC_000007.12:g.128283935A>G	NCBI36
NG_011807.1:g.31217A>G , LRG_870:g.31217A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.7379A>G (FLNC) MANE Select	ENSP00000327145.8:p.Asp2460Gly
ENST00000325888.12:c.7379A>G (FLNC)	ENSP00000327145.8:p.Asp2460Gly
ENST00000346177.6:c.7280A>G (FLNC)	ENSP00000344002.6:p.Asp2427Gly
NM_001127487.1:c.7280A>G (FLNC)	NP_001120959.1:p.Asp2427Gly
NM_001458.4:c.7379A>G , LRG_870t1:c.7379A>G (FLNC)	NP_001449.3:p.Asp2460Gly
NR_149055.1:n.103-3248T>C (FLNC-AS1)
NM_001127487.2:c.7280A>G (FLNC)	NP_001120959.1:p.Asp2427Gly
NM_001458.5:c.7379A>G (FLNC) MANE Select	NP_001449.3:p.Asp2460Gly