Canonical Allele Identifier: CA166195187
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs918950376
MyVariant Identifiers: chr7:g.128497111_128497134del (hg19) chr7:g.128857057_128857080del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857059_128857082del , CM000669.2:g.128857059_128857082del GRCh38
NC_000007.13:g.128497113_128497136del , CM000669.1:g.128497113_128497136del GRCh37
NC_000007.12:g.128284349_128284372del NCBI36
NG_011807.1:g.31631_31654del , LRG_870:g.31631_31654del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7562-59_7562-36del (FLNC) MANE Select ENSP00000327145.8:n.7562-59_7562-36del
ENST00000325888.12:c.7562-59_7562-36del (FLNC) ENSP00000327145.8:n.7562-59_7562-36del
ENST00000346177.6:c.7463-59_7463-36del (FLNC) ENSP00000344002.6:n.7463-59_7463-36del
NM_001127487.1:c.7463-59_7463-36del (FLNC) NP_001120959.1:n.7463-59_7463-36del
NM_001458.4:c.7562-59_7562-36del , LRG_870t1:c.7562-59_7562-36del (FLNC) NP_001449.3:n.7562-59_7562-36del
NR_149055.1:n.103-3683_103-3660del (FLNC-AS1)
NM_001127487.2:c.7463-59_7463-36del (FLNC) NP_001120959.1:n.7463-59_7463-36del
NM_001458.5:c.7562-59_7562-36del (FLNC) MANE Select NP_001449.3:n.7562-59_7562-36del
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