Canonical Allele Identifier: CA658657718
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 478125
ClinVar RCV Id: RCV000541523
dbSNP Id: rs1554398674

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842784_128842810del , CM000669.2:g.128842784_128842810del GRCh38
NC_000007.13:g.128482838_128482864del , CM000669.1:g.128482838_128482864del GRCh37
NC_000007.12:g.128270074_128270100del NCBI36
NG_011807.1:g.17356_17382del , LRG_870:g.17356_17382del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2390-10_2406del
ENST00000325888.12:c.2390-10_2406del
ENST00000346177.6:c.2390-10_2406del
ENST00000388853.3:n.506-10_522del
NM_001127487.1:c.2390-10_2406del
NM_001458.4:c.2390-10_2406del , LRG_870t1:c.2390-10_2406del
NM_001127487.2:c.2390-10_2406del
NM_001458.5:c.2390-10_2406del