Canonical Allele Identifier: CA2684820645
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858553_128858565del , CM000669.2:g.128858553_128858565del GRCh38
NC_000007.13:g.128498607_128498619del , CM000669.1:g.128498607_128498619del GRCh37
NC_000007.12:g.128285843_128285855del NCBI36
NG_011807.1:g.33125_33137del , LRG_870:g.33125_33137del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*30_*42del (FLNC) MANE Select ENSP00000327145.8:n.*30_*42del
ENST00000325888.12:c.*30_*42del (FLNC) ENSP00000327145.8:n.*30_*42del
ENST00000346177.6:c.*30_*42del (FLNC) ENSP00000344002.6:n.*30_*42del
NM_001127487.1:c.*30_*42del (FLNC) NP_001120959.1:n.*30_*42del
NM_001458.4:c.*30_*42del , LRG_870t1:c.*30_*42del (FLNC) NP_001449.3:n.*30_*42del
NR_149055.1:n.102+3965_102+3977del (FLNC-AS1)
NM_001127487.2:c.*30_*42del (FLNC) NP_001120959.1:n.*30_*42del
NM_001458.5:c.*30_*42del (FLNC) MANE Select NP_001449.3:n.*30_*42del