Canonical Allele Identifier: CA1107055639
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs1808701087
gnomAD v3: 7-128849213-C-A
gnomAD v4: 7-128849213-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849213C>A , CM000669.2:g.128849213C>A GRCh38
NC_000007.13:g.128489267C>A , CM000669.1:g.128489267C>A GRCh37
NC_000007.12:g.128276503C>A NCBI36
NG_011807.1:g.23785C>A , LRG_870:g.23785C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4951+9C>A MANE Select ENSP00000327145.8:n.4951+9C>A
ENST00000325888.12:c.4951+9C>A ENSP00000327145.8:n.4951+9C>A
ENST00000346177.6:c.4951+9C>A ENSP00000344002.6:n.4951+9C>A
NM_001127487.1:c.4951+9C>A NP_001120959.1:n.4951+9C>A
NM_001458.4:c.4951+9C>A , LRG_870t1:c.4951+9C>A NP_001449.3:n.4951+9C>A
NM_001127487.2:c.4951+9C>A NP_001120959.1:n.4951+9C>A
NM_001458.5:c.4951+9C>A MANE Select NP_001449.3:n.4951+9C>A
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