Canonical Allele Identifier: CA10559988

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154351689G>A , CM000685.2:g.154351689G>A	GRCh38
NC_000023.10:g.153580057G>A , CM000685.1:g.153580057G>A	GRCh37
NC_000023.9:g.153233251G>A	NCBI36
NG_011506.1:g.27950C>T
NG_011506.2:g.27950C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.6915C>T MANE Select	NP_001104026.1:p.Tyr2305=
ENST00000369850.10:c.6915C>T MANE Select	ENSP00000358866.3:p.Tyr2305=
NM_001110556.1:c.6915C>T	NP_001104026.1:p.Tyr2305=
NM_001456.3:c.6891C>T	NP_001447.2:p.Tyr2297=
NM_001456.4:c.6891C>T	NP_001447.2:p.Tyr2297=
ENST00000344736.8:c.6795C>T	ENSP00000358863.3:p.Tyr2265=
ENST00000360319.8:c.6891C>T	ENSP00000353467.4:p.Tyr2297=
ENST00000360319.9:c.6891C>T	ENSP00000353467.4:p.Tyr2297=
ENST00000369850.7:c.6915C>T	ENSP00000358866.3:p.Tyr2305=
ENST00000369856.7:c.6834C>T	ENSP00000358872.4:p.Tyr2278=
ENST00000369856.8:c.6834C>T	ENSP00000358872.4:p.Tyr2278=
ENST00000420627.5:c.6871C>T	ENSP00000408921.1:n.6871C>T
ENST00000422373.5:c.6891C>T	ENSP00000416926.1:p.Tyr2297=
ENST00000422373.6:c.3696C>T	ENSP00000416926.2:p.Tyr1232=
ENST00000444578.1:c.735C>T	ENSP00000397824.1:p.Tyr245=
ENST00000490936.5:n.2904C>T
ENST00000498411.1:n.67+1128C>T
ENST00000610817.4:c.5919C>T	ENSP00000480593.1:p.Tyr1973=
ENST00000610817.5:c.6972C>T	ENSP00000480593.2:n.6972C>T
ENST00000673639.2:c.280-2999C>T
ENST00000676696.1:c.7194C>T	ENSP00000503392.1:n.7194C>T
ENST00000678304.1:n.2094C>T
XM_011531127.1:c.6819C>T	XP_011529429.1:p.Tyr2273=
XM_011531128.1:c.6795C>T	XP_011529430.1:p.Tyr2265=
XM_011531129.1:c.6741C>T	XP_011529431.1:p.Tyr2247=
XM_011531130.1:c.6717C>T	XP_011529432.1:p.Tyr2239=
XM_011531131.1:c.6714C>T	XP_011529433.1:p.Tyr2238=