Canonical Allele Identifier: CA2684820359
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128857404-C-CT
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857404_128857405insT , CM000669.2:g.128857404_128857405insT GRCh38
NC_000007.13:g.128497458_128497459insT , CM000669.1:g.128497458_128497459insT GRCh37
NC_000007.12:g.128284694_128284695insT NCBI36
NG_011807.1:g.31976_31977insT , LRG_870:g.31976_31977insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7780+68_7780+69insT (FLNC) MANE Select ENSP00000327145.8:n.7780+68_7780+69insT
ENST00000325888.12:c.7780+68_7780+69insT (FLNC) ENSP00000327145.8:n.7780+68_7780+69insT
ENST00000346177.6:c.7681+68_7681+69insT (FLNC) ENSP00000344002.6:n.7681+68_7681+69insT
NM_001127487.1:c.7681+68_7681+69insT (FLNC) NP_001120959.1:n.7681+68_7681+69insT
NM_001458.4:c.7780+68_7780+69insT , LRG_870t1:c.7780+68_7780+69insT (FLNC) NP_001449.3:n.7780+68_7780+69insT
NR_149055.1:n.103-4008_103-4007insA (FLNC-AS1)
NM_001127487.2:c.7681+68_7681+69insT (FLNC) NP_001120959.1:n.7681+68_7681+69insT
NM_001458.5:c.7780+68_7780+69insT (FLNC) MANE Select NP_001449.3:n.7780+68_7780+69insT
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