Canonical Allele Identifier: CA457849585

Gene: FLNC FLNC-AS1

Linked Data

• ClinVar Variation Id: 2067847
• ClinVar RCV Id: RCV002970701
• MyVariant Identifiers: chr7:g.128493869T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128853815T>C , CM000669.2:g.128853815T>C	GRCh38
NC_000007.13:g.128493869T>C , CM000669.1:g.128493869T>C	GRCh37
NC_000007.12:g.128281105T>C	NCBI36
NG_011807.1:g.28387T>C , LRG_870:g.28387T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6462T>C (FLNC) MANE Select	ENSP00000327145.8:p.Cys2154=
ENST00000325888.12:c.6462T>C (FLNC)	ENSP00000327145.8:p.Cys2154=
ENST00000346177.6:c.6363T>C (FLNC)	ENSP00000344002.6:p.Cys2121=
NM_001127487.1:c.6363T>C (FLNC)	NP_001120959.1:p.Cys2121=
NM_001458.4:c.6462T>C , LRG_870t1:c.6462T>C (FLNC)	NP_001449.3:p.Cys2154=
NR_149055.1:n.103-418A>G (FLNC-AS1)
NM_001127487.2:c.6363T>C (FLNC)	NP_001120959.1:p.Cys2121=
NM_001458.5:c.6462T>C (FLNC) MANE Select	NP_001449.3:p.Cys2154=