Canonical Allele Identifier: CA2684814956
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128853925-TCCTCACCCCTCGCTTCCCTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853934_128853953del , CM000669.2:g.128853934_128853953del GRCh38
NC_000007.13:g.128493988_128494007del , CM000669.1:g.128493988_128494007del GRCh37
NC_000007.12:g.128281224_128281243del NCBI36
NG_011807.1:g.28506_28525del , LRG_870:g.28506_28525del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6485-40_6485-21del (FLNC) MANE Select ENSP00000327145.8:n.6485-40_6485-21del
ENST00000325888.12:c.6485-40_6485-21del (FLNC) ENSP00000327145.8:n.6485-40_6485-21del
ENST00000346177.6:c.6386-40_6386-21del (FLNC) ENSP00000344002.6:n.6386-40_6386-21del
NM_001127487.1:c.6386-40_6386-21del (FLNC) NP_001120959.1:n.6386-40_6386-21del
NM_001458.4:c.6485-40_6485-21del , LRG_870t1:c.6485-40_6485-21del (FLNC) NP_001449.3:n.6485-40_6485-21del
NR_149055.1:n.103-548_103-529del (FLNC-AS1)
NM_001127487.2:c.6386-40_6386-21del (FLNC) NP_001120959.1:n.6386-40_6386-21del
NM_001458.5:c.6485-40_6485-21del (FLNC) MANE Select NP_001449.3:n.6485-40_6485-21del
Search 100 bp 5'
Search 100 bp 3'