Canonical Allele Identifier: CA166212562

Gene: FLNC

Linked Data

• dbSNP Id: rs970517485
• gnomAD v2: 7-128475177-AGAAGCAGCCTTCTGACCGGAAGG-A
• gnomAD v3: 7-128835123-AGAAGCAGCCTTCTGACCGGAAGG-A
• gnomAD v4: 7-128835123-AGAAGCAGCCTTCTGACCGGAAGG-A
• MyVariant Identifiers: chr7:g.128475178_128475200del (hg19) ; chr7:g.128835124_128835146del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128835125_128835147del , CM000669.2:g.128835125_128835147del	GRCh38
NC_000007.13:g.128475179_128475201del , CM000669.1:g.128475179_128475201del	GRCh37
NC_000007.12:g.128262415_128262437del	NCBI36
NG_011807.1:g.9697_9719del , LRG_870:g.9697_9719del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.353-201_353-179del MANE Select	ENSP00000327145.8:n.353-201_353-179del
ENST00000325888.12:c.353-201_353-179del	ENSP00000327145.8:n.353-201_353-179del
ENST00000346177.6:c.353-201_353-179del	ENSP00000344002.6:n.353-201_353-179del
NM_001127487.1:c.353-201_353-179del	NP_001120959.1:n.353-201_353-179del
NM_001458.4:c.353-201_353-179del , LRG_870t1:c.353-201_353-179del	NP_001449.3:n.353-201_353-179del
NM_001127487.2:c.353-201_353-179del	NP_001120959.1:n.353-201_353-179del
NM_001458.5:c.353-201_353-179del MANE Select	NP_001449.3:n.353-201_353-179del