Canonical Allele Identifier: CA1682913320
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128854165del , CM000669.2:g.128854165del GRCh38
NC_000007.13:g.128494219del , CM000669.1:g.128494219del GRCh37
NC_000007.12:g.128281455del NCBI36
NG_011807.1:g.28737del , LRG_870:g.28737del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.6676del (FLNC) MANE Select ENSP00000327145.8:p.Leu2226TrpfsTer25
ENST00000325888.12:c.6676del (FLNC) ENSP00000327145.8:p.Leu2226TrpfsTer25
ENST00000346177.6:c.6577del (FLNC) ENSP00000344002.6:p.Leu2193TrpfsTer25
NM_001127487.1:c.6577del (FLNC) NP_001120959.1:p.Leu2193TrpfsTer25
NM_001458.4:c.6676del , LRG_870t1:c.6676del (FLNC) NP_001449.3:p.Leu2226TrpfsTer25
NR_149055.1:n.103-767del (FLNC-AS1)
NM_001127487.2:c.6577del (FLNC) NP_001120959.1:p.Leu2193TrpfsTer25
NM_001458.5:c.6676del (FLNC) MANE Select NP_001449.3:p.Leu2226TrpfsTer25
Search 100 bp 5'
Search 100 bp 3'