Canonical Allele Identifier: CA2824282372

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352980_154352990del , CM000685.2:g.154352980_154352990del	GRCh38
NC_000023.10:g.153581348_153581358del , CM000685.1:g.153581348_153581358del	GRCh37
NC_000023.9:g.153234542_153234552del	NCBI36
NG_011506.1:g.26653_26663del
NG_011506.2:g.26653_26663del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6202+15_6202+25del	ENSP00000353467.4:n.6202+15_6202+25del
ENST00000369850.10:c.6226+15_6226+25del MANE Select	ENSP00000358866.3:n.6226+15_6226+25del
ENST00000369856.8:c.6145+15_6145+25del	ENSP00000358872.4:n.6145+15_6145+25del
ENST00000422373.6:c.3161-311_3161-301del	ENSP00000416926.2:n.3161-311_3161-301del
ENST00000610817.5:c.6283+15_6283+25del	ENSP00000480593.2:n.6283+15_6283+25del
ENST00000673639.2:c.280-4296_280-4286del
ENST00000676696.1:c.6505+15_6505+25del	ENSP00000503392.1:n.6505+15_6505+25del
ENST00000678304.1:n.1405+15_1405+25del
ENST00000344736.8:c.6106+15_6106+25del	ENSP00000358863.3:n.6106+15_6106+25del
ENST00000360319.8:c.6202+15_6202+25del	ENSP00000353467.4:n.6202+15_6202+25del
ENST00000369850.7:c.6226+15_6226+25del	ENSP00000358866.3:n.6226+15_6226+25del
ENST00000369856.7:c.6145+15_6145+25del	ENSP00000358872.4:n.6145+15_6145+25del
ENST00000415241.1:c.428+15_428+25del
ENST00000420627.5:c.6182+15_6182+25del	ENSP00000408921.1:n.6182+15_6182+25del
ENST00000422373.5:c.6202+15_6202+25del	ENSP00000416926.1:n.6202+15_6202+25del
ENST00000444578.1:c.169+15_169+25del	ENSP00000397824.1:n.169+15_169+25del
ENST00000466325.1:n.380_390del
ENST00000490936.5:n.2215+15_2215+25del
ENST00000610817.4:c.5844+407_5844+417del	ENSP00000480593.1:n.5844+407_5844+417del
NM_001110556.1:c.6226+15_6226+25del	NP_001104026.1:n.6226+15_6226+25del
NM_001456.3:c.6202+15_6202+25del	NP_001447.2:n.6202+15_6202+25del
XM_011531127.1:c.6130+15_6130+25del	XP_011529429.1:n.6130+15_6130+25del
XM_011531128.1:c.6106+15_6106+25del	XP_011529430.1:n.6106+15_6106+25del
XM_011531129.1:c.6052+15_6052+25del	XP_011529431.1:n.6052+15_6052+25del
XM_011531130.1:c.6028+15_6028+25del	XP_011529432.1:n.6028+15_6028+25del
XM_011531131.1:c.6025+15_6025+25del	XP_011529433.1:n.6025+15_6025+25del
NM_001110556.2:c.6226+15_6226+25del MANE Select	NP_001104026.1:n.6226+15_6226+25del
NM_001456.4:c.6202+15_6202+25del	NP_001447.2:n.6202+15_6202+25del