Canonical Allele Identifier: CA1742578642
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128854027_128854030delinsCGCA , CM000669.2:g.128854027_128854030delinsCGCA GRCh38
NC_000007.13:g.128494081_128494084delinsCGCA , CM000669.1:g.128494081_128494084delinsCGCA GRCh37
NC_000007.12:g.128281317_128281320delinsCGCA NCBI36
NG_011807.1:g.28599_28602delinsCGCA , LRG_870:g.28599_28602delinsCGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6538_6541delinsCGCA (FLNC) MANE Select ENSP00000327145.8:p.Arg2180=
ENST00000325888.12:c.6538_6541delinsCGCA (FLNC) ENSP00000327145.8:p.Arg2180=
ENST00000346177.6:c.6439_6442delinsCGCA (FLNC) ENSP00000344002.6:p.Arg2147=
NM_001127487.1:c.6439_6442delinsCGCA (FLNC) NP_001120959.1:p.Arg2147=
NM_001458.4:c.6538_6541delinsCGCA , LRG_870t1:c.6538_6541delinsCGCA (FLNC) NP_001449.3:p.Arg2180=
NR_149055.1:n.103-633_103-630delinsTGCG (FLNC-AS1)
NM_001127487.2:c.6439_6442delinsCGCA (FLNC) NP_001120959.1:p.Arg2147=
NM_001458.5:c.6538_6541delinsCGCA (FLNC) MANE Select NP_001449.3:p.Arg2180=