Canonical Allele Identifier: CA457849281
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1156637
ClinVar RCV Id: RCV001499415
dbSNP Id: rs752263141
MyVariant Identifiers: chr7:g.128491654G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851600G>C , CM000669.2:g.128851600G>C GRCh38
NC_000007.13:g.128491654G>C , CM000669.1:g.128491654G>C GRCh37
NC_000007.12:g.128278890G>C NCBI36
NG_011807.1:g.26172G>C , LRG_870:g.26172G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.5814G>C (FLNC) MANE Select ENSP00000327145.8:p.Pro1938=
ENST00000325888.12:c.5814G>C (FLNC) ENSP00000327145.8:p.Pro1938=
ENST00000346177.6:c.5715G>C (FLNC) ENSP00000344002.6:p.Pro1905=
NM_001127487.1:c.5715G>C (FLNC) NP_001120959.1:p.Pro1905=
NM_001458.4:c.5814G>C , LRG_870t1:c.5814G>C (FLNC) NP_001449.3:p.Pro1938=
NR_149055.1:n.216-100C>G (FLNC-AS1)
NM_001127487.2:c.5715G>C (FLNC) NP_001120959.1:p.Pro1905=
NM_001458.5:c.5814G>C (FLNC) MANE Select NP_001449.3:p.Pro1938=
Search 100 bp 5'
Search 100 bp 3'