Canonical Allele Identifier: CA369227397
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539418
dbSNP Id: rs1554398369

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841290A>C , CM000669.2:g.128841290A>C GRCh38
NC_000007.13:g.128481344A>C , CM000669.1:g.128481344A>C GRCh37
NC_000007.12:g.128268580A>C NCBI36
NG_011807.1:g.15862A>C , LRG_870:g.15862A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1934A>C MANE Select ENSP00000327145.8:p.Asp645Ala
ENST00000325888.12:c.1934A>C ENSP00000327145.8:p.Asp645Ala
ENST00000346177.6:c.1934A>C ENSP00000344002.6:p.Asp645Ala
NM_001127487.1:c.1934A>C NP_001120959.1:p.Asp645Ala
NM_001458.4:c.1934A>C , LRG_870t1:c.1934A>C NP_001449.3:p.Asp645Ala
NM_001127487.2:c.1934A>C NP_001120959.1:p.Asp645Ala
NM_001458.5:c.1934A>C MANE Select NP_001449.3:p.Asp645Ala