Canonical Allele Identifier: CA578150164

Gene: FLNC

Linked Data

• gnomAD v2: 7-128481059-CG-C
• gnomAD v4: 7-128841005-CG-C
• MyVariant Identifiers: chr7:g.128481060del (hg19) ; chr7:g.128841006del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128841010del , CM000669.2:g.128841010del	GRCh38
NC_000007.13:g.128481064del , CM000669.1:g.128481064del	GRCh37
NC_000007.12:g.128268300del	NCBI36
NG_011807.1:g.15582del , LRG_870:g.15582del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1813+40del MANE Select	ENSP00000327145.8:n.1813+40del
ENST00000325888.12:c.1813+40del	ENSP00000327145.8:n.1813+40del
ENST00000346177.6:c.1813+40del	ENSP00000344002.6:n.1813+40del
NM_001127487.1:c.1813+40del	NP_001120959.1:n.1813+40del
NM_001458.4:c.1813+40del , LRG_870t1:c.1813+40del	NP_001449.3:n.1813+40del
NM_001127487.2:c.1813+40del	NP_001120959.1:n.1813+40del
NM_001458.5:c.1813+40del MANE Select	NP_001449.3:n.1813+40del