Canonical Allele Identifier: CA369201161
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2938150
ClinVar RCV Id: RCV003796972
dbSNP Id: rs1489699318
gnomAD v2: 7-128487780-G-A
gnomAD v4: 7-128847726-G-A
MyVariant Identifiers: chr7:g.128487780G>A (hg19) chr7:g.128847726G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128847726G>A , CM000669.2:g.128847726G>A GRCh38
NC_000007.13:g.128487780G>A , CM000669.1:g.128487780G>A GRCh37
NC_000007.12:g.128275016G>A NCBI36
NG_011807.1:g.22298G>A , LRG_870:g.22298G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.4318G>A MANE Select ENSP00000327145.8:p.Val1440Met
ENST00000325888.12:c.4318G>A ENSP00000327145.8:p.Val1440Met
ENST00000346177.6:c.4318G>A ENSP00000344002.6:p.Val1440Met
NM_001127487.1:c.4318G>A NP_001120959.1:p.Val1440Met
NM_001458.4:c.4318G>A , LRG_870t1:c.4318G>A NP_001449.3:p.Val1440Met
NM_001127487.2:c.4318G>A NP_001120959.1:p.Val1440Met
NM_001458.5:c.4318G>A MANE Select NP_001449.3:p.Val1440Met
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