Canonical Allele Identifier: CA1139532401
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128844867_128844868dup , CM000669.2:g.128844867_128844868dup GRCh38
NC_000007.13:g.128484921_128484922dup , CM000669.1:g.128484921_128484922dup GRCh37
NC_000007.12:g.128272157_128272158dup NCBI36
NG_011807.1:g.19439_19440dup , LRG_870:g.19439_19440dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.3402_3403dup MANE Select ENSP00000327145.8:p.Phe1135CysfsTer?
ENST00000325888.12:c.3402_3403dup ENSP00000327145.8:p.Phe1135CysfsTer?
ENST00000346177.6:c.3402_3403dup ENSP00000344002.6:p.Phe1135CysfsTer?
NM_001127487.1:c.3402_3403dup NP_001120959.1:p.Phe1135CysfsTer?
NM_001458.4:c.3402_3403dup , LRG_870t1:c.3402_3403dup NP_001449.3:p.Phe1135CysfsTer?
NM_001127487.2:c.3402_3403dup NP_001120959.1:p.Phe1135CysfsTer?
NM_001458.5:c.3402_3403dup MANE Select NP_001449.3:p.Phe1135CysfsTer?