Canonical Allele Identifier: CA2695208446
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128852974_128852984del , CM000669.2:g.128852974_128852984del GRCh38
NC_000007.13:g.128493028_128493038del , CM000669.1:g.128493028_128493038del GRCh37
NC_000007.12:g.128280264_128280274del NCBI36
NG_011807.1:g.27546_27556del , LRG_870:g.27546_27556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6151_6161del (FLNC) MANE Select ENSP00000327145.8:p.Leu2051ThrfsTer25
ENST00000325888.12:c.6151_6161del (FLNC) ENSP00000327145.8:p.Leu2051ThrfsTer25
ENST00000346177.6:c.6052_6062del (FLNC) ENSP00000344002.6:p.Leu2018ThrfsTer25
NM_001127487.1:c.6052_6062del (FLNC) NP_001120959.1:p.Leu2018ThrfsTer25
NM_001458.4:c.6151_6161del , LRG_870t1:c.6151_6161del (FLNC) NP_001449.3:p.Leu2051ThrfsTer25
NR_149055.1:n.215+304_215+314del (FLNC-AS1)
NM_001127487.2:c.6052_6062del (FLNC) NP_001120959.1:p.Leu2018ThrfsTer25
NM_001458.5:c.6151_6161del (FLNC) MANE Select NP_001449.3:p.Leu2051ThrfsTer25