Canonical Allele Identifier: CA10559809

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154348885G>A , CM000685.2:g.154348885G>A	GRCh38
NC_000023.10:g.153577253G>A , CM000685.1:g.153577253G>A	GRCh37
NC_000023.9:g.153230447G>A	NCBI36
NG_011506.1:g.30754C>T
NG_011506.2:g.30754C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7884C>T	ENSP00000353467.4:p.His2628=
ENST00000369850.10:c.7908C>T MANE Select	ENSP00000358866.3:p.His2636=
ENST00000369856.8:c.7827C>T	ENSP00000358872.4:p.His2609=
ENST00000422373.6:c.4689C>T	ENSP00000416926.2:p.His1563=
ENST00000610817.5:c.7965C>T	ENSP00000480593.2:n.7965C>T
ENST00000673639.2:c.280-195C>T
ENST00000676696.1:c.8187C>T	ENSP00000503392.1:n.8187C>T
ENST00000678304.1:n.3626C>T
ENST00000344736.8:c.7788C>T	ENSP00000358863.3:p.His2596=
ENST00000360319.8:c.7884C>T	ENSP00000353467.4:p.His2628=
ENST00000369850.7:c.7908C>T	ENSP00000358866.3:p.His2636=
ENST00000369856.7:c.7827C>T	ENSP00000358872.4:p.His2609=
ENST00000420627.5:c.7864C>T	ENSP00000408921.1:n.7864C>T
ENST00000422373.5:c.7884C>T	ENSP00000416926.1:p.His2628=
ENST00000490936.5:n.5137C>T
ENST00000498411.1:n.68-55C>T
ENST00000610817.4:c.6912C>T	ENSP00000480593.1:p.His2304=
NM_001110556.1:c.7908C>T	NP_001104026.1:p.His2636=
NM_001456.3:c.7884C>T	NP_001447.2:p.His2628=
XM_011531127.1:c.7812C>T	XP_011529429.1:p.His2604=
XM_011531128.1:c.7788C>T	XP_011529430.1:p.His2596=
XM_011531129.1:c.7734C>T	XP_011529431.1:p.His2578=
XM_011531130.1:c.7710C>T	XP_011529432.1:p.His2570=
XM_011531131.1:c.7707C>T	XP_011529433.1:p.His2569=
NM_001110556.2:c.7908C>T MANE Select	NP_001104026.1:p.His2636=
NM_001456.4:c.7884C>T	NP_001447.2:p.His2628=