Canonical Allele Identifier: CA10560366

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154354812del , CM000685.2:g.154354812del	GRCh38
NC_000023.10:g.153583180del , CM000685.1:g.153583180del	GRCh37
NC_000023.9:g.153236374del	NCBI36
NG_011506.1:g.24832del
NG_011506.2:g.24832del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5193+18del	ENSP00000353467.4:n.5193+18del
ENST00000369850.10:c.5217+18del MANE Select	ENSP00000358866.3:n.5217+18del
ENST00000369856.8:c.5136+18del	ENSP00000358872.4:n.5136+18del
ENST00000422373.6:c.3161-2132del	ENSP00000416926.2:n.3161-2132del
ENST00000610817.5:c.5274+18del	ENSP00000480593.2:n.5274+18del
ENST00000673639.2:c.280-6117del
ENST00000676696.1:c.5496+18del	ENSP00000503392.1:n.5496+18del
ENST00000678304.1:n.396+18del
ENST00000344736.8:c.5193+18del	ENSP00000358863.3:n.5193+18del
ENST00000360319.8:c.5193+18del	ENSP00000353467.4:n.5193+18del
ENST00000369850.7:c.5217+18del	ENSP00000358866.3:n.5217+18del
ENST00000369856.7:c.5136+18del	ENSP00000358872.4:n.5136+18del
ENST00000420627.5:c.5173+18del	ENSP00000408921.1:n.5173+18del
ENST00000422373.5:c.5193+18del	ENSP00000416926.1:n.5193+18del
ENST00000438732.2:c.65+18del
ENST00000490936.5:n.1206+18del
ENST00000610817.4:c.5136+18del	ENSP00000480593.1:n.5136+18del
NM_001110556.1:c.5217+18del	NP_001104026.1:n.5217+18del
NM_001456.3:c.5193+18del	NP_001447.2:n.5193+18del
XM_011531127.1:c.5217+18del	XP_011529429.1:n.5217+18del
XM_011531128.1:c.5193+18del	XP_011529430.1:n.5193+18del
XM_011531129.1:c.5217+18del	XP_011529431.1:n.5217+18del
XM_011531130.1:c.5193+18del	XP_011529432.1:n.5193+18del
XM_011531131.1:c.5016+18del	XP_011529433.1:n.5016+18del
NM_001110556.2:c.5217+18del MANE Select	NP_001104026.1:n.5217+18del
NM_001456.4:c.5193+18del	NP_001447.2:n.5193+18del