Canonical Allele Identifier: CA4474853
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs369532954
ExAC: 7:128483661 C / A
gnomAD v2: 7-128483661-C-A
gnomAD v3: 7-128843607-C-A
gnomAD v4: 7-128843607-C-A
MyVariant Identifiers: chr7:g.128483661C>A (hg19) chr7:g.128483661_128483662delinsAG (hg19) chr7:g.128843607C>A (hg38) chr7:g.128843607_128843608delinsAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843607C>A , CM000669.2:g.128843607C>A GRCh38
NC_000007.13:g.128483661C>A , CM000669.1:g.128483661C>A GRCh37
NC_000007.12:g.128270897C>A NCBI36
NG_011807.1:g.18179C>A , LRG_870:g.18179C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2811+30C>A MANE Select ENSP00000327145.8:n.2811+30C>A
ENST00000325888.12:c.2811+30C>A ENSP00000327145.8:n.2811+30C>A
ENST00000346177.6:c.2811+30C>A ENSP00000344002.6:n.2811+30C>A
NM_001127487.1:c.2811+30C>A NP_001120959.1:n.2811+30C>A
NM_001458.4:c.2811+30C>A , LRG_870t1:c.2811+30C>A NP_001449.3:n.2811+30C>A
NM_001127487.2:c.2811+30C>A NP_001120959.1:n.2811+30C>A
NM_001458.5:c.2811+30C>A MANE Select NP_001449.3:n.2811+30C>A
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