Canonical Allele Identifier: CA2684813277

Gene: FLNC FLNC-AS1

Linked Data

• gnomAD v4: 7-128852789-GGCCCACAGGATGCTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128852793_128852808del , CM000669.2:g.128852793_128852808del	GRCh38
NC_000007.13:g.128492847_128492862del , CM000669.1:g.128492847_128492862del	GRCh37
NC_000007.12:g.128280083_128280098del	NCBI36
NG_011807.1:g.27365_27380del , LRG_870:g.27365_27380del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325888.13:c.6005-35_6005-20del (FLNC) MANE Select	ENSP00000327145.8:n.6005-35_6005-20del
ENST00000325888.12:c.6005-35_6005-20del (FLNC)	ENSP00000327145.8:n.6005-35_6005-20del
ENST00000346177.6:c.5906-35_5906-20del (FLNC)	ENSP00000344002.6:n.5906-35_5906-20del
NM_001127487.1:c.5906-35_5906-20del (FLNC)	NP_001120959.1:n.5906-35_5906-20del
NM_001458.4:c.6005-35_6005-20del , LRG_870t1:c.6005-35_6005-20del (FLNC)	NP_001449.3:n.6005-35_6005-20del
NR_149055.1:n.215+480_215+495del (FLNC-AS1)
NM_001127487.2:c.5906-35_5906-20del (FLNC)	NP_001120959.1:n.5906-35_5906-20del
NM_001458.5:c.6005-35_6005-20del (FLNC) MANE Select	NP_001449.3:n.6005-35_6005-20del