Canonical Allele Identifier: CA2684812617
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128851599-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128851603del , CM000669.2:g.128851603del GRCh38
NC_000007.13:g.128491657del , CM000669.1:g.128491657del GRCh37
NC_000007.12:g.128278893del NCBI36
NG_011807.1:g.26175del , LRG_870:g.26175del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.5817del (FLNC) MANE Select ENSP00000327145.8:p.Ser1940AlafsTer13
ENST00000325888.12:c.5817del (FLNC) ENSP00000327145.8:p.Ser1940AlafsTer13
ENST00000346177.6:c.5718del (FLNC) ENSP00000344002.6:p.Ser1907AlafsTer13
NM_001127487.1:c.5718del (FLNC) NP_001120959.1:p.Ser1907AlafsTer13
NM_001458.4:c.5817del , LRG_870t1:c.5817del (FLNC) NP_001449.3:p.Ser1940AlafsTer13
NR_149055.1:n.216-100del (FLNC-AS1)
NM_001127487.2:c.5718del (FLNC) NP_001120959.1:p.Ser1907AlafsTer13
NM_001458.5:c.5817del (FLNC) MANE Select NP_001449.3:p.Ser1940AlafsTer13
Search 100 bp 5'
Search 100 bp 3'