Canonical Allele Identifier: CA833141099

Gene: FLNC

Linked Data

• dbSNP Id: rs1397936849
• gnomAD v3: 7-128835073-C-CA
• gnomAD v4: 7-128835073-C-CA
• MyVariant Identifiers: chr7:g.128475127_128475128insA (hg19) ; chr7:g.128835073_128835074insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128835074dup , CM000669.2:g.128835074dup	GRCh38
NC_000007.13:g.128475128dup , CM000669.1:g.128475128dup	GRCh37
NC_000007.12:g.128262364dup	NCBI36
NG_011807.1:g.9646dup , LRG_870:g.9646dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.353-252dup MANE Select	ENSP00000327145.8:n.353-252dup
ENST00000325888.12:c.353-252dup	ENSP00000327145.8:n.353-252dup
ENST00000346177.6:c.353-252dup	ENSP00000344002.6:n.353-252dup
NM_001127487.1:c.353-252dup	NP_001120959.1:n.353-252dup
NM_001458.4:c.353-252dup , LRG_870t1:c.353-252dup	NP_001449.3:n.353-252dup
NM_001127487.2:c.353-252dup	NP_001120959.1:n.353-252dup
NM_001458.5:c.353-252dup MANE Select	NP_001449.3:n.353-252dup