Canonical Allele Identifier: CA4475857

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs779609448
• ExAC: 7:128492833 CAG / C
• gnomAD v2: 7-128492833-CAG-C
• gnomAD v3: 7-128852779-CAG-C
• gnomAD v4: 7-128852779-CAG-C
• MyVariant Identifiers: chr7:g.128492834_128492835del (hg19) ; chr7:g.128852780_128852781del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128852780_128852781del , CM000669.2:g.128852780_128852781del	GRCh38
NC_000007.13:g.128492834_128492835del , CM000669.1:g.128492834_128492835del	GRCh37
NC_000007.12:g.128280070_128280071del	NCBI36
NG_011807.1:g.27352_27353del , LRG_870:g.27352_27353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6004+28_6004+29del (FLNC) MANE Select	ENSP00000327145.8:n.6004+28_6004+29del
ENST00000325888.12:c.6004+28_6004+29del (FLNC)	ENSP00000327145.8:n.6004+28_6004+29del
ENST00000346177.6:c.5905+28_5905+29del (FLNC)	ENSP00000344002.6:n.5905+28_5905+29del
NM_001127487.1:c.5905+28_5905+29del (FLNC)	NP_001120959.1:n.5905+28_5905+29del
NM_001458.4:c.6004+28_6004+29del , LRG_870t1:c.6004+28_6004+29del (FLNC)	NP_001449.3:n.6004+28_6004+29del
NR_149055.1:n.215+504_215+505del (FLNC-AS1)
NM_001127487.2:c.5905+28_5905+29del (FLNC)	NP_001120959.1:n.5905+28_5905+29del
NM_001458.5:c.6004+28_6004+29del (FLNC) MANE Select	NP_001449.3:n.6004+28_6004+29del