Canonical Allele Identifier: CA4476328
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 539429
dbSNP Id: rs746349463

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857174G>C , CM000669.2:g.128857174G>C GRCh38
NC_000007.13:g.128497228G>C , CM000669.1:g.128497228G>C GRCh37
NC_000007.12:g.128284464G>C NCBI36
NG_011807.1:g.31746G>C , LRG_870:g.31746G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7618G>C (FLNC) MANE Select ENSP00000327145.8:p.Val2540Leu
ENST00000325888.12:c.7618G>C (FLNC) ENSP00000327145.8:p.Val2540Leu
ENST00000346177.6:c.7519G>C (FLNC) ENSP00000344002.6:p.Val2507Leu
NM_001127487.1:c.7519G>C (FLNC) NP_001120959.1:p.Val2507Leu
NM_001458.4:c.7618G>C , LRG_870t1:c.7618G>C (FLNC) NP_001449.3:p.Val2540Leu
NR_149055.1:n.103-3777C>G (FLNC-AS1)
NM_001127487.2:c.7519G>C (FLNC) NP_001120959.1:p.Val2507Leu
NM_001458.5:c.7618G>C (FLNC) MANE Select NP_001449.3:p.Val2540Leu