Canonical Allele Identifier: CA2684820630
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128858363-A-ACGGCCCCAAGACC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858365_128858377dup , CM000669.2:g.128858365_128858377dup GRCh38
NC_000007.13:g.128498419_128498431dup , CM000669.1:g.128498419_128498431dup GRCh37
NC_000007.12:g.128285655_128285667dup NCBI36
NG_011807.1:g.32937_32949dup , LRG_870:g.32937_32949dup

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.8020_8032dup (FLNC) MANE Select ENSP00000327145.8:p.Pro2678ArgfsTer7
ENST00000325888.12:c.8020_8032dup (FLNC) ENSP00000327145.8:p.Pro2678ArgfsTer7
ENST00000346177.6:c.7921_7933dup (FLNC) ENSP00000344002.6:p.Pro2645ArgfsTer7
NM_001127487.1:c.7921_7933dup (FLNC) NP_001120959.1:p.Pro2645ArgfsTer7
NM_001458.4:c.8020_8032dup , LRG_870t1:c.8020_8032dup (FLNC) NP_001449.3:p.Pro2678ArgfsTer7
NR_149055.1:n.102+4149_102+4161dup (FLNC-AS1)
NM_001127487.2:c.7921_7933dup (FLNC) NP_001120959.1:p.Pro2645ArgfsTer7
NM_001458.5:c.8020_8032dup (FLNC) MANE Select NP_001449.3:p.Pro2678ArgfsTer7
Search 100 bp 5'
Search 100 bp 3'