Canonical Allele Identifier: CA2695237724

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353309dup , CM000685.2:g.154353309dup	GRCh38
NC_000023.10:g.153581677dup , CM000685.1:g.153581677dup	GRCh37
NC_000023.9:g.153234871dup	NCBI36
NG_011506.1:g.26330dup
NG_011506.2:g.26330dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5985dup	ENSP00000353467.4:p.Asn1996Ter
ENST00000369850.10:c.6009dup MANE Select	ENSP00000358866.3:p.Asn2004Ter
ENST00000369856.8:c.5928dup	ENSP00000358872.4:p.Asn1977Ter
ENST00000422373.6:c.3161-634dup	ENSP00000416926.2:n.3161-634dup
ENST00000610817.5:c.6066dup	ENSP00000480593.2:n.6066dup
ENST00000673639.2:c.280-4619dup
ENST00000676696.1:c.6288dup	ENSP00000503392.1:n.6288dup
ENST00000678304.1:n.1188dup
ENST00000344736.8:c.5889dup	ENSP00000358863.3:p.Asn1964Ter
ENST00000360319.8:c.5985dup	ENSP00000353467.4:p.Asn1996Ter
ENST00000369850.7:c.6009dup	ENSP00000358866.3:p.Asn2004Ter
ENST00000369856.7:c.5928dup	ENSP00000358872.4:p.Asn1977Ter
ENST00000415241.1:c.194dup
ENST00000420627.5:c.5965dup	ENSP00000408921.1:n.5965dup
ENST00000422373.5:c.5985dup	ENSP00000416926.1:p.Asn1996Ter
ENST00000438732.2:c.683dup
ENST00000466325.1:n.148dup
ENST00000490936.5:n.1998dup
ENST00000610817.4:c.5844+84dup	ENSP00000480593.1:n.5844+84dup
NM_001110556.1:c.6009dup	NP_001104026.1:p.Asn2004Ter
NM_001456.3:c.5985dup	NP_001447.2:p.Asn1996Ter
XM_011531127.1:c.5913dup	XP_011529429.1:p.Asn1972Ter
XM_011531128.1:c.5889dup	XP_011529430.1:p.Asn1964Ter
XM_011531129.1:c.5835dup	XP_011529431.1:p.Asn1946Ter
XM_011531130.1:c.5811dup	XP_011529432.1:p.Asn1938Ter
XM_011531131.1:c.5808dup	XP_011529433.1:p.Asn1937Ter
NM_001110556.2:c.6009dup MANE Select	NP_001104026.1:p.Asn2004Ter
NM_001456.4:c.5985dup	NP_001447.2:p.Asn1996Ter