Canonical Allele Identifier: CA2684820301
Gene: FLNC HGNC NCBI
FLNC-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-128857060-AGTCCCTCTTGGGCCACAAGCC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128857061_128857081del , CM000669.2:g.128857061_128857081del GRCh38
NC_000007.13:g.128497115_128497135del , CM000669.1:g.128497115_128497135del GRCh37
NC_000007.12:g.128284351_128284371del NCBI36
NG_011807.1:g.31633_31653del , LRG_870:g.31633_31653del

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.7562-57_7562-37del (FLNC) MANE Select ENSP00000327145.8:n.7562-57_7562-37del
ENST00000325888.12:c.7562-57_7562-37del (FLNC) ENSP00000327145.8:n.7562-57_7562-37del
ENST00000346177.6:c.7463-57_7463-37del (FLNC) ENSP00000344002.6:n.7463-57_7463-37del
NM_001127487.1:c.7463-57_7463-37del (FLNC) NP_001120959.1:n.7463-57_7463-37del
NM_001458.4:c.7562-57_7562-37del , LRG_870t1:c.7562-57_7562-37del (FLNC) NP_001449.3:n.7562-57_7562-37del
NR_149055.1:n.103-3684_103-3664del (FLNC-AS1)
NM_001127487.2:c.7463-57_7463-37del (FLNC) NP_001120959.1:n.7463-57_7463-37del
NM_001458.5:c.7562-57_7562-37del (FLNC) MANE Select NP_001449.3:n.7562-57_7562-37del
Search 100 bp 5'
Search 100 bp 3'