Canonical Allele Identifier: CA577747480

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1313092957
• gnomAD v2: 7-128497485-CCA-C
• gnomAD v3: 7-128857431-CCA-C
• gnomAD v4: 7-128857431-CCA-C
• MyVariant Identifiers: chr7:g.128497486_128497487del (hg19) ; chr7:g.128857432_128857433del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857432_128857433del , CM000669.2:g.128857432_128857433del	GRCh38
NC_000007.13:g.128497486_128497487del , CM000669.1:g.128497486_128497487del	GRCh37
NC_000007.12:g.128284722_128284723del	NCBI36
NG_011807.1:g.32004_32005del , LRG_870:g.32004_32005del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7780+96_7780+97del (FLNC) MANE Select	ENSP00000327145.8:n.7780+96_7780+97del
ENST00000325888.12:c.7780+96_7780+97del (FLNC)	ENSP00000327145.8:n.7780+96_7780+97del
ENST00000346177.6:c.7681+96_7681+97del (FLNC)	ENSP00000344002.6:n.7681+96_7681+97del
NM_001127487.1:c.7681+96_7681+97del (FLNC)	NP_001120959.1:n.7681+96_7681+97del
NM_001458.4:c.7780+96_7780+97del , LRG_870t1:c.7780+96_7780+97del (FLNC)	NP_001449.3:n.7780+96_7780+97del
NR_149055.1:n.103-4036_103-4035del (FLNC-AS1)
NM_001127487.2:c.7681+96_7681+97del (FLNC)	NP_001120959.1:n.7681+96_7681+97del
NM_001458.5:c.7780+96_7780+97del (FLNC) MANE Select	NP_001449.3:n.7780+96_7780+97del