Canonical Allele Identifier: CA1742578317
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs577503639

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128853889C>G , CM000669.2:g.128853889C>G GRCh38
NC_000007.13:g.128493943C>G , CM000669.1:g.128493943C>G GRCh37
NC_000007.12:g.128281179C>G NCBI36
NG_011807.1:g.28461C>G , LRG_870:g.28461C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.6484+52C>G (FLNC) MANE Select ENSP00000327145.8:n.6484+52C>G
ENST00000325888.12:c.6484+52C>G (FLNC) ENSP00000327145.8:n.6484+52C>G
ENST00000346177.6:c.6385+52C>G (FLNC) ENSP00000344002.6:n.6385+52C>G
NM_001127487.1:c.6385+52C>G (FLNC) NP_001120959.1:n.6385+52C>G
NM_001458.4:c.6484+52C>G , LRG_870t1:c.6484+52C>G (FLNC) NP_001449.3:n.6484+52C>G
NR_149055.1:n.103-492G>C (FLNC-AS1)
NM_001127487.2:c.6385+52C>G (FLNC) NP_001120959.1:n.6385+52C>G
NM_001458.5:c.6484+52C>G (FLNC) MANE Select NP_001449.3:n.6484+52C>G