Canonical Allele Identifier: CA2842842105

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154358322dup , CM000685.2:g.154358322dup	GRCh38
NC_000023.10:g.153586690dup , CM000685.1:g.153586690dup	GRCh37
NC_000023.9:g.153239884dup	NCBI36
NG_011506.1:g.21317dup
NG_011506.2:g.21317dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.4632dup	ENSP00000353467.4:p.Ala1545CysfsTer?
ENST00000369850.10:c.4632dup MANE Select	ENSP00000358866.3:p.Ala1545CysfsTer?
ENST00000369856.8:c.4551dup	ENSP00000358872.4:p.Ala1518CysfsTer?
ENST00000422373.6:c.3160+3033dup	ENSP00000416926.2:n.3160+3033dup
ENST00000610817.5:c.4689dup	ENSP00000480593.2:n.4689dup
ENST00000673639.2:c.279+7114dup
ENST00000676696.1:c.4911dup	ENSP00000503392.1:n.4911dup
ENST00000678304.1:n.148+767dup
ENST00000344736.8:c.4632dup	ENSP00000358863.3:p.Ala1545CysfsTer?
ENST00000360319.8:c.4632dup	ENSP00000353467.4:p.Ala1545CysfsTer?
ENST00000369850.7:c.4632dup	ENSP00000358866.3:p.Ala1545CysfsTer?
ENST00000369856.7:c.4551dup	ENSP00000358872.4:p.Ala1518CysfsTer?
ENST00000420627.5:c.4588dup	ENSP00000408921.1:n.4588dup
ENST00000422373.5:c.4632dup	ENSP00000416926.1:p.Ala1545CysfsTer?
ENST00000466319.1:n.254dup
ENST00000490936.5:n.645dup
ENST00000610817.4:c.4551dup	ENSP00000480593.1:p.Ala1518CysfsTer?
NM_001110556.1:c.4632dup	NP_001104026.1:p.Ala1545CysfsTer?
NM_001456.3:c.4632dup	NP_001447.2:p.Ala1545CysfsTer?
XM_011531127.1:c.4632dup	XP_011529429.1:p.Ala1545CysfsTer?
XM_011531128.1:c.4632dup	XP_011529430.1:p.Ala1545CysfsTer?
XM_011531129.1:c.4632dup	XP_011529431.1:p.Ala1545CysfsTer?
XM_011531130.1:c.4632dup	XP_011529432.1:p.Ala1545CysfsTer?
XM_011531131.1:c.4431dup	XP_011529433.1:p.Ala1478CysfsTer?
NM_001110556.2:c.4632dup MANE Select	NP_001104026.1:p.Ala1545CysfsTer?
NM_001456.4:c.4632dup	NP_001447.2:p.Ala1545CysfsTer?