Canonical Allele Identifier: CA4474168
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472188
ClinVar RCV Id: RCV000550419 RCV002377142
dbSNP Id: rs763968152
ExAC: 7:128477759 G / A
gnomAD v2: 7-128477759-G-A
gnomAD v3: 7-128837705-G-A
gnomAD v4: 7-128837705-G-A
COSMIC: COSM2769297
MyVariant Identifiers: chr7:g.128477759G>A (hg19) chr7:g.128837705G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128837705G>A , CM000669.2:g.128837705G>A GRCh38
NC_000007.13:g.128477759G>A , CM000669.1:g.128477759G>A GRCh37
NC_000007.12:g.128264995G>A NCBI36
NG_011807.1:g.12277G>A , LRG_870:g.12277G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.919G>A MANE Select ENSP00000327145.8:p.Val307Met
ENST00000325888.12:c.919G>A ENSP00000327145.8:p.Val307Met
ENST00000346177.6:c.919G>A ENSP00000344002.6:p.Val307Met
NM_001127487.1:c.919G>A NP_001120959.1:p.Val307Met
NM_001458.4:c.919G>A , LRG_870t1:c.919G>A NP_001449.3:p.Val307Met
NM_001127487.2:c.919G>A NP_001120959.1:p.Val307Met
NM_001458.5:c.919G>A MANE Select NP_001449.3:p.Val307Met
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Search 100 bp 3'