Canonical Allele Identifier: CA2684812638
Gene: FLNC HGNC NCBI

Linked Data

gnomAD v4: 7-128841108-G-GC
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841109dup , CM000669.2:g.128841109dup GRCh38
NC_000007.13:g.128481163dup , CM000669.1:g.128481163dup GRCh37
NC_000007.12:g.128268399dup NCBI36
NG_011807.1:g.15681dup , LRG_870:g.15681dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1814-61dup MANE Select ENSP00000327145.8:n.1814-61dup
ENST00000325888.12:c.1814-61dup ENSP00000327145.8:n.1814-61dup
ENST00000346177.6:c.1814-61dup ENSP00000344002.6:n.1814-61dup
NM_001127487.1:c.1814-61dup NP_001120959.1:n.1814-61dup
NM_001458.4:c.1814-61dup , LRG_870t1:c.1814-61dup NP_001449.3:n.1814-61dup
NM_001127487.2:c.1814-61dup NP_001120959.1:n.1814-61dup
NM_001458.5:c.1814-61dup MANE Select NP_001449.3:n.1814-61dup
Search 100 bp 5'
Search 100 bp 3'