Canonical Allele Identifier: CA1139768875

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353047del , CM000685.2:g.154353047del	GRCh38
NC_000023.10:g.153581415del , CM000685.1:g.153581415del	GRCh37
NC_000023.9:g.153234609del	NCBI36
NG_011506.1:g.26593del
NG_011506.2:g.26593del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6157del	ENSP00000353467.4:p.His2053ThrfsTer?
ENST00000369850.10:c.6181del MANE Select	ENSP00000358866.3:p.His2061ThrfsTer?
ENST00000369856.8:c.6100del	ENSP00000358872.4:p.His2034ThrfsTer?
ENST00000422373.6:c.3161-371del	ENSP00000416926.2:n.3161-371del
ENST00000610817.5:c.6238del	ENSP00000480593.2:n.6238del
ENST00000673639.2:c.280-4356del
ENST00000676696.1:c.6460del	ENSP00000503392.1:n.6460del
ENST00000678304.1:n.1360del
ENST00000344736.8:c.6061del	ENSP00000358863.3:p.His2021ThrfsTer?
ENST00000360319.8:c.6157del	ENSP00000353467.4:p.His2053ThrfsTer?
ENST00000369850.7:c.6181del	ENSP00000358866.3:p.His2061ThrfsTer?
ENST00000369856.7:c.6100del	ENSP00000358872.4:p.His2034ThrfsTer?
ENST00000415241.1:c.383del
ENST00000420627.5:c.6137del	ENSP00000408921.1:n.6137del
ENST00000422373.5:c.6157del	ENSP00000416926.1:p.His2053ThrfsTer?
ENST00000444578.1:c.124del	ENSP00000397824.1:p.His42ThrfsTer?
ENST00000466325.1:n.320del
ENST00000490936.5:n.2170del
ENST00000610817.4:c.5844+347del	ENSP00000480593.1:n.5844+347del
NM_001110556.1:c.6181del	NP_001104026.1:p.His2061ThrfsTer?
NM_001456.3:c.6157del	NP_001447.2:p.His2053ThrfsTer?
XM_011531127.1:c.6085del	XP_011529429.1:p.His2029ThrfsTer?
XM_011531128.1:c.6061del	XP_011529430.1:p.His2021ThrfsTer?
XM_011531129.1:c.6007del	XP_011529431.1:p.His2003ThrfsTer?
XM_011531130.1:c.5983del	XP_011529432.1:p.His1995ThrfsTer?
XM_011531131.1:c.5980del	XP_011529433.1:p.His1994ThrfsTer?
NM_001110556.2:c.6181del MANE Select	NP_001104026.1:p.His2061ThrfsTer?
NM_001456.4:c.6157del	NP_001447.2:p.His2053ThrfsTer?