Canonical Allele Identifier: CA2684820732
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128858599-A-ACAC
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858599_128858600insCAC , CM000669.2:g.128858599_128858600insCAC GRCh38
NC_000007.13:g.128498653_128498654insCAC , CM000669.1:g.128498653_128498654insCAC GRCh37
NC_000007.12:g.128285889_128285890insCAC NCBI36
NG_011807.1:g.33171_33172insCAC , LRG_870:g.33171_33172insCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*76_*77insCAC (FLNC) MANE Select ENSP00000327145.8:n.*76_*77insCAC
ENST00000325888.12:c.*76_*77insCAC (FLNC) ENSP00000327145.8:n.*76_*77insCAC
ENST00000346177.6:c.*76_*77insCAC (FLNC) ENSP00000344002.6:n.*76_*77insCAC
NM_001127487.1:c.*76_*77insCAC (FLNC) NP_001120959.1:n.*76_*77insCAC
NM_001458.4:c.*76_*77insCAC , LRG_870t1:c.*76_*77insCAC (FLNC) NP_001449.3:n.*76_*77insCAC
NR_149055.1:n.102+3925_102+3926insGTG (FLNC-AS1)
NM_001127487.2:c.*76_*77insCAC (FLNC) NP_001120959.1:n.*76_*77insCAC
NM_001458.5:c.*76_*77insCAC (FLNC) MANE Select NP_001449.3:n.*76_*77insCAC
Search 100 bp 5'
Search 100 bp 3'