Canonical Allele Identifier: CA1742568476
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841193C= , CM000669.2:g.128841193C= GRCh38
NC_000007.13:g.128481247C= , CM000669.1:g.128481247C= GRCh37
NC_000007.12:g.128268483C= NCBI36
NG_011807.1:g.15765C= , LRG_870:g.15765C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1837C= MANE Select ENSP00000327145.8:p.Gln613=
ENST00000325888.12:c.1837C= ENSP00000327145.8:p.Gln613=
ENST00000346177.6:c.1837C= ENSP00000344002.6:p.Gln613=
NM_001127487.1:c.1837C= NP_001120959.1:p.Gln613=
NM_001458.4:c.1837C= , LRG_870t1:c.1837C= NP_001449.3:p.Gln613=
NM_001127487.2:c.1837C= NP_001120959.1:p.Gln613=
NM_001458.5:c.1837C= MANE Select NP_001449.3:p.Gln613=