Canonical Allele Identifier: CA2579014822
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858159del , CM000669.2:g.128858159del GRCh38
NC_000007.13:g.128498213del , CM000669.1:g.128498213del GRCh37
NC_000007.12:g.128285449del NCBI36
NG_011807.1:g.32731del , LRG_870:g.32731del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7932del (FLNC) MANE Select ENSP00000327145.8:p.Leu2645CysfsTer23
ENST00000325888.12:c.7932del (FLNC) ENSP00000327145.8:p.Leu2645CysfsTer23
ENST00000346177.6:c.7833del (FLNC) ENSP00000344002.6:p.Leu2612CysfsTer23
NM_001127487.1:c.7833del (FLNC) NP_001120959.1:p.Leu2612CysfsTer23
NM_001458.4:c.7932del , LRG_870t1:c.7932del (FLNC) NP_001449.3:p.Leu2645CysfsTer23
NR_149055.1:n.102+4368del (FLNC-AS1)
NM_001127487.2:c.7833del (FLNC) NP_001120959.1:p.Leu2612CysfsTer23
NM_001458.5:c.7932del (FLNC) MANE Select NP_001449.3:p.Leu2645CysfsTer23