Canonical Allele Identifier: CA833134803

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1357241229
• gnomAD v3: 7-128856676-TC-T
• gnomAD v4: 7-128856676-TC-T
• MyVariant Identifiers: chr7:g.128496731del (hg19) ; chr7:g.128856677del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128856679del , CM000669.2:g.128856679del	GRCh38
NC_000007.13:g.128496733del , CM000669.1:g.128496733del	GRCh37
NC_000007.12:g.128283969del	NCBI36
NG_011807.1:g.31251del , LRG_870:g.31251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7384+29del (FLNC) MANE Select	ENSP00000327145.8:n.7384+29del
ENST00000325888.12:c.7384+29del (FLNC)	ENSP00000327145.8:n.7384+29del
ENST00000346177.6:c.7285+29del (FLNC)	ENSP00000344002.6:n.7285+29del
NM_001127487.1:c.7285+29del (FLNC)	NP_001120959.1:n.7285+29del
NM_001458.4:c.7384+29del , LRG_870t1:c.7384+29del (FLNC)	NP_001449.3:n.7384+29del
NR_149055.1:n.103-3280del (FLNC-AS1)
NM_001127487.2:c.7285+29del (FLNC)	NP_001120959.1:n.7285+29del
NM_001458.5:c.7384+29del (FLNC) MANE Select	NP_001449.3:n.7384+29del