Canonical Allele Identifier: CA2684819296
Gene: FLNC HGNC NCBI

Linked Data

gnomAD v4: 7-128835314-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128835318del , CM000669.2:g.128835318del GRCh38
NC_000007.13:g.128475372del , CM000669.1:g.128475372del GRCh37
NC_000007.12:g.128262608del NCBI36
NG_011807.1:g.9890del , LRG_870:g.9890del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.353-8del MANE Select ENSP00000327145.8:n.353-8del
ENST00000325888.12:c.353-8del ENSP00000327145.8:n.353-8del
ENST00000346177.6:c.353-8del ENSP00000344002.6:n.353-8del
NM_001127487.1:c.353-8del NP_001120959.1:n.353-8del
NM_001458.4:c.353-8del , LRG_870t1:c.353-8del NP_001449.3:n.353-8del
NM_001127487.2:c.353-8del NP_001120959.1:n.353-8del
NM_001458.5:c.353-8del MANE Select NP_001449.3:n.353-8del
Search 100 bp 5'
Search 100 bp 3'