Canonical Allele Identifier: CA2684820634
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858544_128858556del , CM000669.2:g.128858544_128858556del GRCh38
NC_000007.13:g.128498598_128498610del , CM000669.1:g.128498598_128498610del GRCh37
NC_000007.12:g.128285834_128285846del NCBI36
NG_011807.1:g.33116_33128del , LRG_870:g.33116_33128del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*21_*33del (FLNC) MANE Select ENSP00000327145.8:n.*21_*33del
ENST00000325888.12:c.*21_*33del (FLNC) ENSP00000327145.8:n.*21_*33del
ENST00000346177.6:c.*21_*33del (FLNC) ENSP00000344002.6:n.*21_*33del
NM_001127487.1:c.*21_*33del (FLNC) NP_001120959.1:n.*21_*33del
NM_001458.4:c.*21_*33del , LRG_870t1:c.*21_*33del (FLNC) NP_001449.3:n.*21_*33del
NR_149055.1:n.102+3974_102+3986del (FLNC-AS1)
NM_001127487.2:c.*21_*33del (FLNC) NP_001120959.1:n.*21_*33del
NM_001458.5:c.*21_*33del (FLNC) MANE Select NP_001449.3:n.*21_*33del