Canonical Allele Identifier: CA369219422
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128497238A>T (hg19) chr7:g.128857184A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857184A>T , CM000669.2:g.128857184A>T GRCh38
NC_000007.13:g.128497238A>T , CM000669.1:g.128497238A>T GRCh37
NC_000007.12:g.128284474A>T NCBI36
NG_011807.1:g.31756A>T , LRG_870:g.31756A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.7628A>T (FLNC) MANE Select ENSP00000327145.8:p.Asp2543Val
ENST00000325888.12:c.7628A>T (FLNC) ENSP00000327145.8:p.Asp2543Val
ENST00000346177.6:c.7529A>T (FLNC) ENSP00000344002.6:p.Asp2510Val
NM_001127487.1:c.7529A>T (FLNC) NP_001120959.1:p.Asp2510Val
NM_001458.4:c.7628A>T , LRG_870t1:c.7628A>T (FLNC) NP_001449.3:p.Asp2543Val
NR_149055.1:n.103-3787T>A (FLNC-AS1)
NM_001127487.2:c.7529A>T (FLNC) NP_001120959.1:p.Asp2510Val
NM_001458.5:c.7628A>T (FLNC) MANE Select NP_001449.3:p.Asp2543Val
Search 100 bp 5'
Search 100 bp 3'