Canonical Allele Identifier: CA2843472323
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128858418dup , CM000669.2:g.128858418dup GRCh38
NC_000007.13:g.128498472dup , CM000669.1:g.128498472dup GRCh37
NC_000007.12:g.128285708dup NCBI36
NG_011807.1:g.32990dup , LRG_870:g.32990dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.8073dup (FLNC) MANE Select ENSP00000327145.8:p.Tyr2692ValfsTer21
ENST00000325888.12:c.8073dup (FLNC) ENSP00000327145.8:p.Tyr2692ValfsTer21
ENST00000346177.6:c.7974dup (FLNC) ENSP00000344002.6:p.Tyr2659ValfsTer21
NM_001127487.1:c.7974dup (FLNC) NP_001120959.1:p.Tyr2659ValfsTer21
NM_001458.4:c.8073dup , LRG_870t1:c.8073dup (FLNC) NP_001449.3:p.Tyr2692ValfsTer21
NR_149055.1:n.102+4107dup (FLNC-AS1)
NM_001127487.2:c.7974dup (FLNC) NP_001120959.1:p.Tyr2659ValfsTer21
NM_001458.5:c.8073dup (FLNC) MANE Select NP_001449.3:p.Tyr2692ValfsTer21