Canonical Allele Identifier: CA658820776

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58136099_58136101del , CM000665.2:g.58136099_58136101del	GRCh38
NC_000003.11:g.58121826_58121828del , CM000665.1:g.58121826_58121828del	GRCh37
NC_000003.10:g.58096866_58096868del	NCBI36
NG_012801.1:g.132700_132702del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.216_218del
ENST00000682868.1:n.6834_6836del
ENST00000682871.1:c.4885_4887del	ENSP00000507805.1:p.Asp1629del
ENST00000684506.1:c.*3417_*3419del	ENSP00000507728.1:n.*3417_*3419del
ENST00000684607.1:c.4885_4887del	ENSP00000508224.1:p.Asp1629del
ENST00000295956.9:c.4792_4794del MANE Select	ENSP00000295956.5:p.Asp1598del
ENST00000295956.8:c.4792_4794del	ENSP00000295956.4:p.Asp1598del
ENST00000358537.7:c.4792_4794del	ENSP00000351339.3:p.Asp1598del
ENST00000429972.6:c.4792_4794del	ENSP00000415599.2:p.Asp1598del
ENST00000481470.5:n.1132_1134del
ENST00000490882.5:c.4885_4887del	ENSP00000420213.1:p.Asp1629del
ENST00000493452.5:c.4285_4287del	ENSP00000418510.1:p.Asp1429del
NM_001164317.1:c.4885_4887del	NP_001157789.1:p.Asp1629del
NM_001164318.1:c.4792_4794del	NP_001157790.1:p.Asp1598del
NM_001164319.1:c.4792_4794del	NP_001157791.1:p.Asp1598del
NM_001457.3:c.4792_4794del	NP_001448.2:p.Asp1598del
XM_005264977.1:c.4885_4887del	XP_005265034.1:p.Asp1629del
XM_005264978.1:c.4885_4887del	XP_005265035.1:p.Asp1629del
XM_005264981.1:c.4885_4887del	XP_005265038.1:p.Asp1629del
XR_940396.1:n.5030_5032del
XM_005264978.2:c.4885_4887del	XP_005265035.1:p.Asp1629del
XR_001740065.1:n.5030_5032del
XR_940396.2:n.5030_5032del
NM_001164317.2:c.4885_4887del	NP_001157789.1:p.Asp1629del
NM_001164318.2:c.4792_4794del	NP_001157790.1:p.Asp1598del
NM_001164319.2:c.4792_4794del	NP_001157791.1:p.Asp1598del
NM_001457.4:c.4792_4794del MANE Select	NP_001448.2:p.Asp1598del