Canonical Allele Identifier: CA2684812591

Gene: FLNC

Linked Data

• dbSNP Id: rs2128935165
• gnomAD v4: 7-128841027-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128841030_128841031del , CM000669.2:g.128841030_128841031del	GRCh38
NC_000007.13:g.128481084_128481085del , CM000669.1:g.128481084_128481085del	GRCh37
NC_000007.12:g.128268320_128268321del	NCBI36
NG_011807.1:g.15602_15603del , LRG_870:g.15602_15603del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.1813+60_1813+61del MANE Select	ENSP00000327145.8:n.1813+60_1813+61del
ENST00000325888.12:c.1813+60_1813+61del	ENSP00000327145.8:n.1813+60_1813+61del
ENST00000346177.6:c.1813+60_1813+61del	ENSP00000344002.6:n.1813+60_1813+61del
NM_001127487.1:c.1813+60_1813+61del	NP_001120959.1:n.1813+60_1813+61del
NM_001458.4:c.1813+60_1813+61del , LRG_870t1:c.1813+60_1813+61del	NP_001449.3:n.1813+60_1813+61del
NM_001127487.2:c.1813+60_1813+61del	NP_001120959.1:n.1813+60_1813+61del
NM_001458.5:c.1813+60_1813+61del MANE Select	NP_001449.3:n.1813+60_1813+61del