Canonical Allele Identifier: CA1742577904
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128842863A= , CM000669.2:g.128842863A= GRCh38
NC_000007.13:g.128482917A= , CM000669.1:g.128482917A= GRCh37
NC_000007.12:g.128270153A= NCBI36
NG_011807.1:g.17435A= , LRG_870:g.17435A=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2459A= MANE Select ENSP00000327145.8:p.Asp820=
ENST00000325888.12:c.2459A= ENSP00000327145.8:p.Asp820=
ENST00000346177.6:c.2459A= ENSP00000344002.6:p.Asp820=
NM_001127487.1:c.2459A= NP_001120959.1:p.Asp820=
NM_001458.4:c.2459A= , LRG_870t1:c.2459A= NP_001449.3:p.Asp820=
NM_001127487.2:c.2459A= NP_001120959.1:p.Asp820=
NM_001458.5:c.2459A= MANE Select NP_001449.3:p.Asp820=