Canonical Allele Identifier: CA1742552560
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1809169725

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858542dup , CM000669.2:g.128858542dup GRCh38
NC_000007.13:g.128498596dup , CM000669.1:g.128498596dup GRCh37
NC_000007.12:g.128285832dup NCBI36
NG_011807.1:g.33114dup , LRG_870:g.33114dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.*19dup (FLNC) MANE Select ENSP00000327145.8:n.*19dup
ENST00000325888.12:c.*19dup (FLNC) ENSP00000327145.8:n.*19dup
ENST00000346177.6:c.*19dup (FLNC) ENSP00000344002.6:n.*19dup
NM_001127487.1:c.*19dup (FLNC) NP_001120959.1:n.*19dup
NM_001458.4:c.*19dup , LRG_870t1:c.*19dup (FLNC) NP_001449.3:n.*19dup
NR_149055.1:n.102+3986dup (FLNC-AS1)
NM_001127487.2:c.*19dup (FLNC) NP_001120959.1:n.*19dup
NM_001458.5:c.*19dup (FLNC) MANE Select NP_001449.3:n.*19dup