Canonical Allele Identifier: CA2695208489
Gene: FLNC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843296del , CM000669.2:g.128843296del GRCh38
NC_000007.13:g.128483350del , CM000669.1:g.128483350del GRCh37
NC_000007.12:g.128270586del NCBI36
NG_011807.1:g.17868del , LRG_870:g.17868del

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2618del MANE Select ENSP00000327145.8:p.Glu873GlyfsTer5
ENST00000325888.12:c.2618del ENSP00000327145.8:p.Glu873GlyfsTer5
ENST00000346177.6:c.2618del ENSP00000344002.6:p.Glu873GlyfsTer5
NM_001127487.1:c.2618del NP_001120959.1:p.Glu873GlyfsTer5
NM_001458.4:c.2618del , LRG_870t1:c.2618del NP_001449.3:p.Glu873GlyfsTer5
NM_001127487.2:c.2618del NP_001120959.1:p.Glu873GlyfsTer5
NM_001458.5:c.2618del MANE Select NP_001449.3:p.Glu873GlyfsTer5
Search 100 bp 5'
Search 100 bp 3'