Canonical Allele Identifier: CA2684818179
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128856536-AACCAGCCAGCGTCCTTTGCCGTGCAGCTGAACGGTGCCCGGGGCGTGATTGATGCCCGGGTGCACACACCCTCGGGGGCTGTGGAGGAGTGCTACGTCTCTGAGCTGGACAGTG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856537_128856650del , CM000669.2:g.128856537_128856650del GRCh38
NC_000007.13:g.128496591_128496704del , CM000669.1:g.128496591_128496704del GRCh37
NC_000007.12:g.128283827_128283940del NCBI36
NG_011807.1:g.31109_31222del , LRG_870:g.31109_31222del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7271_7384del (FLNC) MANE Select ENSP00000327145.8:p.Gln2425_Asp2462del
ENST00000325888.12:c.7271_7384del (FLNC) ENSP00000327145.8:p.Gln2425_Asp2462del
ENST00000346177.6:c.7172_7285del (FLNC) ENSP00000344002.6:p.Gln2392_Asp2429del
NM_001127487.1:c.7172_7285del (FLNC) NP_001120959.1:p.Gln2392_Asp2429del
NM_001458.4:c.7271_7384del , LRG_870t1:c.7271_7384del (FLNC) NP_001449.3:p.Gln2425_Asp2462del
NR_149055.1:n.103-3253_103-3140del (FLNC-AS1)
NM_001127487.2:c.7172_7285del (FLNC) NP_001120959.1:p.Gln2392_Asp2429del
NM_001458.5:c.7271_7384del (FLNC) MANE Select NP_001449.3:p.Gln2425_Asp2462del
Search 100 bp 5'
Search 100 bp 3'