Canonical Allele Identifier: CA2684815482
Gene: FLNC HGNC NCBI

Linked Data

gnomAD v4: 7-128843137-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843140del , CM000669.2:g.128843140del GRCh38
NC_000007.13:g.128483194del , CM000669.1:g.128483194del GRCh37
NC_000007.12:g.128270430del NCBI36
NG_011807.1:g.17712del , LRG_870:g.17712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2551-89del MANE Select ENSP00000327145.8:n.2551-89del
ENST00000325888.12:c.2551-89del ENSP00000327145.8:n.2551-89del
ENST00000346177.6:c.2551-89del ENSP00000344002.6:n.2551-89del
NM_001127487.1:c.2551-89del NP_001120959.1:n.2551-89del
NM_001458.4:c.2551-89del , LRG_870t1:c.2551-89del NP_001449.3:n.2551-89del
NM_001127487.2:c.2551-89del NP_001120959.1:n.2551-89del
NM_001458.5:c.2551-89del MANE Select NP_001449.3:n.2551-89del
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