Canonical Allele Identifier: CA1742580525
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843361_128843364delinsGTTA , CM000669.2:g.128843361_128843364delinsGTTA GRCh38
NC_000007.13:g.128483415_128483418delinsGTTA , CM000669.1:g.128483415_128483418delinsGTTA GRCh37
NC_000007.12:g.128270651_128270654delinsGTTA NCBI36
NG_011807.1:g.17933_17936delinsGTTA , LRG_870:g.17933_17936delinsGTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2641+42_2642-44delinsGTTA MANE Select ENSP00000327145.8:n.2641+42_2642-44delinsGTTA
ENST00000325888.12:c.2641+42_2642-44delinsGTTA ENSP00000327145.8:n.2641+42_2642-44delinsGTTA
ENST00000346177.6:c.2641+42_2642-44delinsGTTA ENSP00000344002.6:n.2641+42_2642-44delinsGTTA
NM_001127487.1:c.2641+42_2642-44delinsGTTA NP_001120959.1:n.2641+42_2642-44delinsGTTA
NM_001458.4:c.2641+42_2642-44delinsGTTA , LRG_870t1:c.2641+42_2642-44delinsGTTA NP_001449.3:n.2641+42_2642-44delinsGTTA
NM_001127487.2:c.2641+42_2642-44delinsGTTA NP_001120959.1:n.2641+42_2642-44delinsGTTA
NM_001458.5:c.2641+42_2642-44delinsGTTA MANE Select NP_001449.3:n.2641+42_2642-44delinsGTTA