Canonical Allele Identifier: CA2684818073
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128856473-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128856473G>T , CM000669.2:g.128856473G>T GRCh38
NC_000007.13:g.128496527G>T , CM000669.1:g.128496527G>T GRCh37
NC_000007.12:g.128283763G>T NCBI36
NG_011807.1:g.31045G>T , LRG_870:g.31045G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7252-45G>T (FLNC) MANE Select ENSP00000327145.8:n.7252-45G>T
ENST00000325888.12:c.7252-45G>T (FLNC) ENSP00000327145.8:n.7252-45G>T
ENST00000346177.6:c.7153-45G>T (FLNC) ENSP00000344002.6:n.7153-45G>T
NM_001127487.1:c.7153-45G>T (FLNC) NP_001120959.1:n.7153-45G>T
NM_001458.4:c.7252-45G>T , LRG_870t1:c.7252-45G>T (FLNC) NP_001449.3:n.7252-45G>T
NR_149055.1:n.103-3076C>A (FLNC-AS1)
NM_001127487.2:c.7153-45G>T (FLNC) NP_001120959.1:n.7153-45G>T
NM_001458.5:c.7252-45G>T (FLNC) MANE Select NP_001449.3:n.7252-45G>T
Search 100 bp 5'
Search 100 bp 3'