Canonical Allele Identifier: CA1742580461
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1146208
ClinVar RCV Id: RCV001485370
dbSNP Id: rs1808418675

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843327_128843330del , CM000669.2:g.128843327_128843330del GRCh38
NC_000007.13:g.128483381_128483384del , CM000669.1:g.128483381_128483384del GRCh37
NC_000007.12:g.128270617_128270620del NCBI36
NG_011807.1:g.17899_17902del , LRG_870:g.17899_17902del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.2641+8_2641+11del MANE Select ENSP00000327145.8:n.2641+8_2641+11del
ENST00000325888.12:c.2641+8_2641+11del ENSP00000327145.8:n.2641+8_2641+11del
ENST00000346177.6:c.2641+8_2641+11del ENSP00000344002.6:n.2641+8_2641+11del
NM_001127487.1:c.2641+8_2641+11del NP_001120959.1:n.2641+8_2641+11del
NM_001458.4:c.2641+8_2641+11del , LRG_870t1:c.2641+8_2641+11del NP_001449.3:n.2641+8_2641+11del
NM_001127487.2:c.2641+8_2641+11del NP_001120959.1:n.2641+8_2641+11del
NM_001458.5:c.2641+8_2641+11del MANE Select NP_001449.3:n.2641+8_2641+11del