Canonical Allele Identifier: CA2840039197
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128854183_128854184del , CM000669.2:g.128854183_128854184del GRCh38
NC_000007.13:g.128494237_128494238del , CM000669.1:g.128494237_128494238del GRCh37
NC_000007.12:g.128281473_128281474del NCBI36
NG_011807.1:g.28755_28756del , LRG_870:g.28755_28756del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6694_6695del (FLNC) MANE Select ENSP00000327145.8:p.Gly2232IlefsTer12
ENST00000325888.12:c.6694_6695del (FLNC) ENSP00000327145.8:p.Gly2232IlefsTer12
ENST00000346177.6:c.6595_6596del (FLNC) ENSP00000344002.6:p.Gly2199IlefsTer12
NM_001127487.1:c.6595_6596del (FLNC) NP_001120959.1:p.Gly2199IlefsTer12
NM_001458.4:c.6694_6695del , LRG_870t1:c.6694_6695del (FLNC) NP_001449.3:p.Gly2232IlefsTer12
NR_149055.1:n.103-786_103-785del (FLNC-AS1)
NM_001127487.2:c.6595_6596del (FLNC) NP_001120959.1:p.Gly2199IlefsTer12
NM_001458.5:c.6694_6695del (FLNC) MANE Select NP_001449.3:p.Gly2232IlefsTer12