Canonical Allele Identifier: CA2695208449
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853812_128853813del , CM000669.2:g.128853812_128853813del GRCh38
NC_000007.13:g.128493866_128493867del , CM000669.1:g.128493866_128493867del GRCh37
NC_000007.12:g.128281102_128281103del NCBI36
NG_011807.1:g.28384_28385del , LRG_870:g.28384_28385del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6459_6460del (FLNC) MANE Select ENSP00000327145.8:p.Cys2154Ter
ENST00000325888.12:c.6459_6460del (FLNC) ENSP00000327145.8:p.Cys2154Ter
ENST00000346177.6:c.6360_6361del (FLNC) ENSP00000344002.6:p.Cys2121Ter
NM_001127487.1:c.6360_6361del (FLNC) NP_001120959.1:p.Cys2121Ter
NM_001458.4:c.6459_6460del , LRG_870t1:c.6459_6460del (FLNC) NP_001449.3:p.Cys2154Ter
NR_149055.1:n.103-416_103-415del (FLNC-AS1)
NM_001127487.2:c.6360_6361del (FLNC) NP_001120959.1:p.Cys2121Ter
NM_001458.5:c.6459_6460del (FLNC) MANE Select NP_001449.3:p.Cys2154Ter