Canonical Allele Identifier: CA457848191
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730314
ClinVar RCV Id: RCV002326490
gnomAD v4: 7-128844795-G-A
MyVariant Identifiers: chr7:g.128484849G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128844795G>A , CM000669.2:g.128844795G>A GRCh38
NC_000007.13:g.128484849G>A , CM000669.1:g.128484849G>A GRCh37
NC_000007.12:g.128272085G>A NCBI36
NG_011807.1:g.19367G>A , LRG_870:g.19367G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.3330G>A MANE Select ENSP00000327145.8:p.Gln1110=
ENST00000325888.12:c.3330G>A ENSP00000327145.8:p.Gln1110=
ENST00000346177.6:c.3330G>A ENSP00000344002.6:p.Gln1110=
NM_001127487.1:c.3330G>A NP_001120959.1:p.Gln1110=
NM_001458.4:c.3330G>A , LRG_870t1:c.3330G>A NP_001449.3:p.Gln1110=
NM_001127487.2:c.3330G>A NP_001120959.1:p.Gln1110=
NM_001458.5:c.3330G>A MANE Select NP_001449.3:p.Gln1110=
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Search 100 bp 3'