Canonical Allele Identifier: CA202081

Gene: FLNC

Linked Data

• dbSNP Id: rs794727437
• ExAC: 7:128488776 GTC / G
• gnomAD v2: 7-128488776-GTC-G
• gnomAD v3: 7-128848722-GTC-G
• gnomAD v4: 7-128848722-GTC-G
• MyVariant Identifiers: chr7:g.128488780_128488781del (hg19) ; chr7:g.128488777_128488778del (hg19) ; chr7:g.128848726_128848727del (hg38) ; chr7:g.128848724_128848725del (hg38) ; chr7:g.128848723_128848724del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128848726_128848727del , CM000669.2:g.128848726_128848727del	GRCh38
NC_000007.13:g.128488780_128488781del , CM000669.1:g.128488780_128488781del	GRCh37
NC_000007.12:g.128276016_128276017del	NCBI36
NG_011807.1:g.23298_23299del , LRG_870:g.23298_23299del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325888.13:c.4737+9_4737+10del MANE Select	ENSP00000327145.8:n.4737+9_4737+10del
ENST00000325888.12:c.4737+9_4737+10del	ENSP00000327145.8:n.4737+9_4737+10del
ENST00000346177.6:c.4737+9_4737+10del	ENSP00000344002.6:n.4737+9_4737+10del
NM_001127487.1:c.4737+9_4737+10del	NP_001120959.1:n.4737+9_4737+10del
NM_001458.4:c.4737+9_4737+10del , LRG_870t1:c.4737+9_4737+10del	NP_001449.3:n.4737+9_4737+10del
NM_001127487.2:c.4737+9_4737+10del	NP_001120959.1:n.4737+9_4737+10del
NM_001458.5:c.4737+9_4737+10del MANE Select	NP_001449.3:n.4737+9_4737+10del