Canonical Allele Identifier: CA4475357
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1140552
ClinVar RCV Id: RCV001477658
dbSNP Id: rs373198674
ExAC: 7:128488027 C / T
gnomAD v2: 7-128488027-C-T
gnomAD v3: 7-128847973-C-T
gnomAD v4: 7-128847973-C-T
MyVariant Identifiers: chr7:g.128488027C>T (hg19) chr7:g.128847973C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128847973C>T , CM000669.2:g.128847973C>T GRCh38
NC_000007.13:g.128488027C>T , CM000669.1:g.128488027C>T GRCh37
NC_000007.12:g.128275263C>T NCBI36
NG_011807.1:g.22545C>T , LRG_870:g.22545C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4485C>T MANE Select ENSP00000327145.8:p.Asp1495=
ENST00000325888.12:c.4485C>T ENSP00000327145.8:p.Asp1495=
ENST00000346177.6:c.4485C>T ENSP00000344002.6:p.Asp1495=
NM_001127487.1:c.4485C>T NP_001120959.1:p.Asp1495=
NM_001458.4:c.4485C>T , LRG_870t1:c.4485C>T NP_001449.3:p.Asp1495=
NM_001127487.2:c.4485C>T NP_001120959.1:p.Asp1495=
NM_001458.5:c.4485C>T MANE Select NP_001449.3:p.Asp1495=
Search 100 bp 5'
Search 100 bp 3'