Canonical Allele Identifier: CA2684820402
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857450_128857451insTTAATGATACGGCG , CM000669.2:g.128857450_128857451insTTAATGATACGGCG GRCh38
NC_000007.13:g.128497504_128497505insTTAATGATACGGCG , CM000669.1:g.128497504_128497505insTTAATGATACGGCG GRCh37
NC_000007.12:g.128284740_128284741insTTAATGATACGGCG NCBI36
NG_011807.1:g.32022_32023insTTAATGATACGGCG , LRG_870:g.32022_32023insTTAATGATACGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7780+114_7780+115insTTAATGATACGGCG (FLNC) MANE Select ENSP00000327145.8:n.7780+114_7780+115insTTAATGATACGGCG
ENST00000325888.12:c.7780+114_7780+115insTTAATGATACGGCG (FLNC) ENSP00000327145.8:n.7780+114_7780+115insTTAATGATACGGCG
ENST00000346177.6:c.7681+114_7681+115insTTAATGATACGGCG (FLNC) ENSP00000344002.6:n.7681+114_7681+115insTTAATGATACGGCG
NM_001127487.1:c.7681+114_7681+115insTTAATGATACGGCG (FLNC) NP_001120959.1:n.7681+114_7681+115insTTAATGATACGGCG
NM_001458.4:c.7780+114_7780+115insTTAATGATACGGCG , LRG_870t1:c.7780+114_7780+115insTTAATGATACGGCG (FLNC) NP_001449.3:n.7780+114_7780+115insTTAATGATACGGCG
NR_149055.1:n.103-4054_103-4053insCGCCGTATCATTAA (FLNC-AS1)
NM_001127487.2:c.7681+114_7681+115insTTAATGATACGGCG (FLNC) NP_001120959.1:n.7681+114_7681+115insTTAATGATACGGCG
NM_001458.5:c.7780+114_7780+115insTTAATGATACGGCG (FLNC) MANE Select NP_001449.3:n.7780+114_7780+115insTTAATGATACGGCG