Canonical Allele Identifier: CA369192564
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1376845
ClinVar RCV Id: RCV001888201
dbSNP Id: rs2128935929
gnomAD v4: 7-128843299-G-A
MyVariant Identifiers: chr7:g.128483353G>A (hg19) chr7:g.128843299G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843299G>A , CM000669.2:g.128843299G>A GRCh38
NC_000007.13:g.128483353G>A , CM000669.1:g.128483353G>A GRCh37
NC_000007.12:g.128270589G>A NCBI36
NG_011807.1:g.17871G>A , LRG_870:g.17871G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2621G>A MANE Select ENSP00000327145.8:p.Gly874Asp
ENST00000325888.12:c.2621G>A ENSP00000327145.8:p.Gly874Asp
ENST00000346177.6:c.2621G>A ENSP00000344002.6:p.Gly874Asp
NM_001127487.1:c.2621G>A NP_001120959.1:p.Gly874Asp
NM_001458.4:c.2621G>A , LRG_870t1:c.2621G>A NP_001449.3:p.Gly874Asp
NM_001127487.2:c.2621G>A NP_001120959.1:p.Gly874Asp
NM_001458.5:c.2621G>A MANE Select NP_001449.3:p.Gly874Asp
Search 100 bp 5'
Search 100 bp 3'