Canonical Allele Identifier: CA578151102
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1389943633
gnomAD v2: 7-128495239-GTC-G
gnomAD v4: 7-128855185-GTC-G
MyVariant Identifiers: chr7:g.128495240_128495241del (hg19) chr7:g.128855186_128855187del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128855192_128855193del , CM000669.2:g.128855192_128855193del GRCh38
NC_000007.13:g.128495246_128495247del , CM000669.1:g.128495246_128495247del GRCh37
NC_000007.12:g.128282482_128282483del NCBI36
NG_011807.1:g.29764_29765del , LRG_870:g.29764_29765del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7136-7_7136-6del (FLNC) MANE Select ENSP00000327145.8:n.7136-7_7136-6del
ENST00000325888.12:c.7136-7_7136-6del (FLNC) ENSP00000327145.8:n.7136-7_7136-6del
ENST00000346177.6:c.7037-7_7037-6del (FLNC) ENSP00000344002.6:n.7037-7_7037-6del
NM_001127487.1:c.7037-7_7037-6del (FLNC) NP_001120959.1:n.7037-7_7037-6del
NM_001458.4:c.7136-7_7136-6del , LRG_870t1:c.7136-7_7136-6del (FLNC) NP_001449.3:n.7136-7_7136-6del
NR_149055.1:n.103-1790_103-1789del (FLNC-AS1)
NM_001127487.2:c.7037-7_7037-6del (FLNC) NP_001120959.1:n.7037-7_7037-6del
NM_001458.5:c.7136-7_7136-6del (FLNC) MANE Select NP_001449.3:n.7136-7_7136-6del
Search 100 bp 5'
Search 100 bp 3'