Canonical Allele Identifier: CA369227116
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2123767
ClinVar RCV Id: RCV003055244
gnomAD v4: 7-128840968-T-C
MyVariant Identifiers: chr7:g.128481022T>C (hg19) chr7:g.128840968T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128840968T>C , CM000669.2:g.128840968T>C GRCh38
NC_000007.13:g.128481022T>C , CM000669.1:g.128481022T>C GRCh37
NC_000007.12:g.128268258T>C NCBI36
NG_011807.1:g.15540T>C , LRG_870:g.15540T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1811T>C MANE Select ENSP00000327145.8:p.Leu604Pro
ENST00000325888.12:c.1811T>C ENSP00000327145.8:p.Leu604Pro
ENST00000346177.6:c.1811T>C ENSP00000344002.6:p.Leu604Pro
NM_001127487.1:c.1811T>C NP_001120959.1:p.Leu604Pro
NM_001458.4:c.1811T>C , LRG_870t1:c.1811T>C NP_001449.3:p.Leu604Pro
NM_001127487.2:c.1811T>C NP_001120959.1:p.Leu604Pro
NM_001458.5:c.1811T>C MANE Select NP_001449.3:p.Leu604Pro
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