Canonical Allele Identifier: CA1107053341
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1808863185
gnomAD v3: 7-128852543-GGGC-G
gnomAD v4: 7-128852543-GGGC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852544_128852546del , CM000669.2:g.128852544_128852546del GRCh38
NC_000007.13:g.128492598_128492600del , CM000669.1:g.128492598_128492600del GRCh37
NC_000007.12:g.128279834_128279836del NCBI36
NG_011807.1:g.27116_27118del , LRG_870:g.27116_27118del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5843-47_5843-45del (FLNC) MANE Select ENSP00000327145.8:n.5843-47_5843-45del
ENST00000325888.12:c.5843-47_5843-45del (FLNC) ENSP00000327145.8:n.5843-47_5843-45del
ENST00000346177.6:c.5744-47_5744-45del (FLNC) ENSP00000344002.6:n.5744-47_5744-45del
NM_001127487.1:c.5744-47_5744-45del (FLNC) NP_001120959.1:n.5744-47_5744-45del
NM_001458.4:c.5843-47_5843-45del , LRG_870t1:c.5843-47_5843-45del (FLNC) NP_001449.3:n.5843-47_5843-45del
NR_149055.1:n.215+739_215+741del (FLNC-AS1)
NM_001127487.2:c.5744-47_5744-45del (FLNC) NP_001120959.1:n.5744-47_5744-45del
NM_001458.5:c.5843-47_5843-45del (FLNC) MANE Select NP_001449.3:n.5843-47_5843-45del
Search 100 bp 5'
Search 100 bp 3'