Canonical Allele Identifier: CA2579014773
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857396_128857414del , CM000669.2:g.128857396_128857414del GRCh38
NC_000007.13:g.128497450_128497468del , CM000669.1:g.128497450_128497468del GRCh37
NC_000007.12:g.128284686_128284704del NCBI36
NG_011807.1:g.31968_31986del , LRG_870:g.31968_31986del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7780+60_7780+78del (FLNC) MANE Select ENSP00000327145.8:n.7780+60_7780+78del
ENST00000325888.12:c.7780+60_7780+78del (FLNC) ENSP00000327145.8:n.7780+60_7780+78del
ENST00000346177.6:c.7681+60_7681+78del (FLNC) ENSP00000344002.6:n.7681+60_7681+78del
NM_001127487.1:c.7681+60_7681+78del (FLNC) NP_001120959.1:n.7681+60_7681+78del
NM_001458.4:c.7780+60_7780+78del , LRG_870t1:c.7780+60_7780+78del (FLNC) NP_001449.3:n.7780+60_7780+78del
NR_149055.1:n.103-4015_103-3997del (FLNC-AS1)
NM_001127487.2:c.7681+60_7681+78del (FLNC) NP_001120959.1:n.7681+60_7681+78del
NM_001458.5:c.7780+60_7780+78del (FLNC) MANE Select NP_001449.3:n.7780+60_7780+78del