Canonical Allele Identifier: CA2579014200
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843317_128843318del , CM000669.2:g.128843317_128843318del GRCh38
NC_000007.13:g.128483371_128483372del , CM000669.1:g.128483371_128483372del GRCh37
NC_000007.12:g.128270607_128270608del NCBI36
NG_011807.1:g.17889_17890del , LRG_870:g.17889_17890del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2639_2640del MANE Select ENSP00000327145.8:p.Thr880ArgfsTer?
ENST00000325888.12:c.2639_2640del ENSP00000327145.8:p.Thr880ArgfsTer?
ENST00000346177.6:c.2639_2640del ENSP00000344002.6:p.Thr880ArgfsTer?
NM_001127487.1:c.2639_2640del NP_001120959.1:p.Thr880ArgfsTer?
NM_001458.4:c.2639_2640del , LRG_870t1:c.2639_2640del NP_001449.3:p.Thr880ArgfsTer?
NM_001127487.2:c.2639_2640del NP_001120959.1:p.Thr880ArgfsTer?
NM_001458.5:c.2639_2640del MANE Select NP_001449.3:p.Thr880ArgfsTer?