Canonical Allele Identifier: CA1742545949
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128840152A= , CM000669.2:g.128840152A= GRCh38
NC_000007.13:g.128480206A= , CM000669.1:g.128480206A= GRCh37
NC_000007.12:g.128267442A= NCBI36
NG_011807.1:g.14724A= , LRG_870:g.14724A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1541A= MANE Select ENSP00000327145.8:p.Lys514=
ENST00000325888.12:c.1541A= ENSP00000327145.8:p.Lys514=
ENST00000346177.6:c.1541A= ENSP00000344002.6:p.Lys514=
NM_001127487.1:c.1541A= NP_001120959.1:p.Lys514=
NM_001458.4:c.1541A= , LRG_870t1:c.1541A= NP_001449.3:p.Lys514=
NM_001127487.2:c.1541A= NP_001120959.1:p.Lys514=
NM_001458.5:c.1541A= MANE Select NP_001449.3:p.Lys514=