Canonical Allele Identifier: CA578150582

Gene: FLNC

Linked Data

• dbSNP Id: rs1332515859
• gnomAD v2: 7-128489310-AG-A
• gnomAD v4: 7-128849256-AG-A
• MyVariant Identifiers: chr7:g.128489311del (hg19) ; chr7:g.128849257del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128849261del , CM000669.2:g.128849261del	GRCh38
NC_000007.13:g.128489315del , CM000669.1:g.128489315del	GRCh37
NC_000007.12:g.128276551del	NCBI36
NG_011807.1:g.23833del , LRG_870:g.23833del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.4951+57del MANE Select	ENSP00000327145.8:n.4951+57del
ENST00000325888.12:c.4951+57del	ENSP00000327145.8:n.4951+57del
ENST00000346177.6:c.4951+57del	ENSP00000344002.6:n.4951+57del
NM_001127487.1:c.4951+57del	NP_001120959.1:n.4951+57del
NM_001458.4:c.4951+57del , LRG_870t1:c.4951+57del	NP_001449.3:n.4951+57del
NM_001127487.2:c.4951+57del	NP_001120959.1:n.4951+57del
NM_001458.5:c.4951+57del MANE Select	NP_001449.3:n.4951+57del