Canonical Allele Identifier: CA2684817363
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128855192-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128855192T>C , CM000669.2:g.128855192T>C GRCh38
NC_000007.13:g.128495246T>C , CM000669.1:g.128495246T>C GRCh37
NC_000007.12:g.128282482T>C NCBI36
NG_011807.1:g.29764T>C , LRG_870:g.29764T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7136-7T>C (FLNC) MANE Select ENSP00000327145.8:n.7136-7T>C
ENST00000325888.12:c.7136-7T>C (FLNC) ENSP00000327145.8:n.7136-7T>C
ENST00000346177.6:c.7037-7T>C (FLNC) ENSP00000344002.6:n.7037-7T>C
NM_001127487.1:c.7037-7T>C (FLNC) NP_001120959.1:n.7037-7T>C
NM_001458.4:c.7136-7T>C , LRG_870t1:c.7136-7T>C (FLNC) NP_001449.3:n.7136-7T>C
NR_149055.1:n.103-1795A>G (FLNC-AS1)
NM_001127487.2:c.7037-7T>C (FLNC) NP_001120959.1:n.7037-7T>C
NM_001458.5:c.7136-7T>C (FLNC) MANE Select NP_001449.3:n.7136-7T>C
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