Canonical Allele Identifier: CA2684815647
Gene: FLNC HGNC NCBI

Linked Data

gnomAD v4: 7-128843212-GCCT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843218_128843220del , CM000669.2:g.128843218_128843220del GRCh38
NC_000007.13:g.128483272_128483274del , CM000669.1:g.128483272_128483274del GRCh37
NC_000007.12:g.128270508_128270510del NCBI36
NG_011807.1:g.17790_17792del , LRG_870:g.17790_17792del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2551-11_2551-9del MANE Select ENSP00000327145.8:n.2551-11_2551-9del
ENST00000325888.12:c.2551-11_2551-9del ENSP00000327145.8:n.2551-11_2551-9del
ENST00000346177.6:c.2551-11_2551-9del ENSP00000344002.6:n.2551-11_2551-9del
NM_001127487.1:c.2551-11_2551-9del NP_001120959.1:n.2551-11_2551-9del
NM_001458.4:c.2551-11_2551-9del , LRG_870t1:c.2551-11_2551-9del NP_001449.3:n.2551-11_2551-9del
NM_001127487.2:c.2551-11_2551-9del NP_001120959.1:n.2551-11_2551-9del
NM_001458.5:c.2551-11_2551-9del MANE Select NP_001449.3:n.2551-11_2551-9del
Search 100 bp 5'
Search 100 bp 3'