Canonical Allele Identifier: CA369204432
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1067540
ClinVar RCV Id: RCV001378838 RCV003365377
dbSNP Id: rs1465588989
gnomAD v2: 7-128489633-G-T
gnomAD v3: 7-128849579-G-T
gnomAD v4: 7-128849579-G-T
MyVariant Identifiers: chr7:g.128489633G>T (hg19) chr7:g.128849579G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849579G>T , CM000669.2:g.128849579G>T GRCh38
NC_000007.13:g.128489633G>T , CM000669.1:g.128489633G>T GRCh37
NC_000007.12:g.128276869G>T NCBI36
NG_011807.1:g.24151G>T , LRG_870:g.24151G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5199+1G>T MANE Select ENSP00000327145.8:n.5199+1G>T
ENST00000325888.12:c.5199+1G>T ENSP00000327145.8:n.5199+1G>T
ENST00000346177.6:c.5199+1G>T ENSP00000344002.6:n.5199+1G>T
NM_001127487.1:c.5199+1G>T NP_001120959.1:n.5199+1G>T
NM_001458.4:c.5199+1G>T , LRG_870t1:c.5199+1G>T NP_001449.3:n.5199+1G>T
NM_001127487.2:c.5199+1G>T NP_001120959.1:n.5199+1G>T
NM_001458.5:c.5199+1G>T MANE Select NP_001449.3:n.5199+1G>T
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Search 100 bp 3'