Canonical Allele Identifier: CA10560058

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352338G>A , CM000685.2:g.154352338G>A	GRCh38
NC_000023.10:g.153580706G>A , CM000685.1:g.153580706G>A	GRCh37
NC_000023.9:g.153233900G>A	NCBI36
NG_011506.1:g.27301C>T
NG_011506.2:g.27301C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6588C>T	ENSP00000353467.4:p.Pro2196=
ENST00000369850.10:c.6612C>T MANE Select	ENSP00000358866.3:p.Pro2204=
ENST00000369856.8:c.6531C>T	ENSP00000358872.4:p.Pro2177=
ENST00000422373.6:c.3393C>T	ENSP00000416926.2:p.Pro1131=
ENST00000610817.5:c.6669C>T	ENSP00000480593.2:n.6669C>T
ENST00000673639.2:c.280-3648C>T
ENST00000676696.1:c.6891C>T	ENSP00000503392.1:n.6891C>T
ENST00000678304.1:n.1791C>T
ENST00000344736.8:c.6492C>T	ENSP00000358863.3:p.Pro2164=
ENST00000360319.8:c.6588C>T	ENSP00000353467.4:p.Pro2196=
ENST00000369850.7:c.6612C>T	ENSP00000358866.3:p.Pro2204=
ENST00000369856.7:c.6531C>T	ENSP00000358872.4:p.Pro2177=
ENST00000420627.5:c.6568C>T	ENSP00000408921.1:n.6568C>T
ENST00000422373.5:c.6588C>T	ENSP00000416926.1:p.Pro2196=
ENST00000444578.1:c.432C>T	ENSP00000397824.1:p.Pro144=
ENST00000474358.5:n.245C>T
ENST00000490936.5:n.2601C>T
ENST00000498411.1:n.67+479C>T
ENST00000610817.4:c.5845-388C>T	ENSP00000480593.1:n.5845-388C>T
NM_001110556.1:c.6612C>T	NP_001104026.1:p.Pro2204=
NM_001456.3:c.6588C>T	NP_001447.2:p.Pro2196=
XM_011531127.1:c.6516C>T	XP_011529429.1:p.Pro2172=
XM_011531128.1:c.6492C>T	XP_011529430.1:p.Pro2164=
XM_011531129.1:c.6438C>T	XP_011529431.1:p.Pro2146=
XM_011531130.1:c.6414C>T	XP_011529432.1:p.Pro2138=
XM_011531131.1:c.6411C>T	XP_011529433.1:p.Pro2137=
NM_001110556.2:c.6612C>T MANE Select	NP_001104026.1:p.Pro2204=
NM_001456.4:c.6588C>T	NP_001447.2:p.Pro2196=