Canonical Allele Identifier: CA2756415442

Gene: FLNB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58077562del , CM000665.2:g.58077562del	GRCh38
NC_000003.11:g.58063289del , CM000665.1:g.58063289del	GRCh37
NC_000003.10:g.58038329del	NCBI36
NG_012801.1:g.74163del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682097.1:c.541+268del	ENSP00000508183.1:n.541+268del
ENST00000682868.1:n.684+268del
ENST00000682871.1:c.541+268del	ENSP00000507805.1:n.541+268del
ENST00000682987.1:n.684+268del
ENST00000683511.1:n.700+268del
ENST00000684107.1:c.541+268del	ENSP00000507440.1:n.541+268del
ENST00000684506.1:c.541+268del	ENSP00000507728.1:n.541+268del
ENST00000684517.1:c.541+268del	ENSP00000507828.1:n.541+268del
ENST00000684607.1:c.541+268del	ENSP00000508224.1:n.541+268del
ENST00000295956.9:c.541+268del MANE Select	ENSP00000295956.5:n.541+268del
ENST00000295956.8:c.541+268del	ENSP00000295956.4:n.541+268del
ENST00000358537.7:c.541+268del	ENSP00000351339.3:n.541+268del
ENST00000429972.6:c.541+268del	ENSP00000415599.2:n.541+268del
ENST00000490882.5:c.541+268del	ENSP00000420213.1:n.541+268del
NM_001164317.1:c.541+268del	NP_001157789.1:n.541+268del
NM_001164318.1:c.541+268del	NP_001157790.1:n.541+268del
NM_001164319.1:c.541+268del	NP_001157791.1:n.541+268del
NM_001457.3:c.541+268del	NP_001448.2:n.541+268del
XM_005264977.1:c.541+268del	XP_005265034.1:n.541+268del
XM_005264978.1:c.541+268del	XP_005265035.1:n.541+268del
XM_005264981.1:c.541+268del	XP_005265038.1:n.541+268del
XR_940396.1:n.686+268del
XM_005264978.2:c.541+268del	XP_005265035.1:n.541+268del
XR_001740065.1:n.686+268del
XR_940396.2:n.686+268del
NM_001164317.2:c.541+268del	NP_001157789.1:n.541+268del
NM_001164318.2:c.541+268del	NP_001157790.1:n.541+268del
NM_001164319.2:c.541+268del	NP_001157791.1:n.541+268del
NM_001457.4:c.541+268del MANE Select	NP_001448.2:n.541+268del