Canonical Allele Identifier: CA577747473

Gene: FLNC FLNC-AS1

Linked Data

• dbSNP Id: rs1271611000
• gnomAD v2: 7-128497416-ACCCAGCCTGCAGCCCAG-A
• gnomAD v4: 7-128857362-ACCCAGCCTGCAGCCCAG-A
• MyVariant Identifiers: chr7:g.128497417_128497433del (hg19) ; chr7:g.128857363_128857379del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128857372_128857388del , CM000669.2:g.128857372_128857388del	GRCh38
NC_000007.13:g.128497426_128497442del , CM000669.1:g.128497426_128497442del	GRCh37
NC_000007.12:g.128284662_128284678del	NCBI36
NG_011807.1:g.31944_31960del , LRG_870:g.31944_31960del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.7780+36_7780+52del (FLNC) MANE Select	ENSP00000327145.8:n.7780+36_7780+52del
ENST00000325888.12:c.7780+36_7780+52del (FLNC)	ENSP00000327145.8:n.7780+36_7780+52del
ENST00000346177.6:c.7681+36_7681+52del (FLNC)	ENSP00000344002.6:n.7681+36_7681+52del
NM_001127487.1:c.7681+36_7681+52del (FLNC)	NP_001120959.1:n.7681+36_7681+52del
NM_001458.4:c.7780+36_7780+52del , LRG_870t1:c.7780+36_7780+52del (FLNC)	NP_001449.3:n.7780+36_7780+52del
NR_149055.1:n.103-3982_103-3966del (FLNC-AS1)
NM_001127487.2:c.7681+36_7681+52del (FLNC)	NP_001120959.1:n.7681+36_7681+52del
NM_001458.5:c.7780+36_7780+52del (FLNC) MANE Select	NP_001449.3:n.7780+36_7780+52del