Canonical Allele Identifier: CA415197209

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581696C>A (hg19) ; chrX:g.154353328C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353328C>A , CM000685.2:g.154353328C>A	GRCh38
NC_000023.10:g.153581696C>A , CM000685.1:g.153581696C>A	GRCh37
NC_000023.9:g.153234890C>A	NCBI36
NG_011506.1:g.26311G>T
NG_011506.2:g.26311G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5966G>T	ENSP00000353467.4:p.Cys1989Phe
ENST00000369850.10:c.5990G>T MANE Select	ENSP00000358866.3:p.Cys1997Phe
ENST00000369856.8:c.5909G>T	ENSP00000358872.4:p.Cys1970Phe
ENST00000422373.6:c.3161-653G>T	ENSP00000416926.2:n.3161-653G>T
ENST00000610817.5:c.6047G>T	ENSP00000480593.2:n.6047G>T
ENST00000673639.2:c.280-4638G>T
ENST00000676696.1:c.6269G>T	ENSP00000503392.1:n.6269G>T
ENST00000678304.1:n.1169G>T
ENST00000344736.8:c.5870G>T	ENSP00000358863.3:p.Cys1957Phe
ENST00000360319.8:c.5966G>T	ENSP00000353467.4:p.Cys1989Phe
ENST00000369850.7:c.5990G>T	ENSP00000358866.3:p.Cys1997Phe
ENST00000369856.7:c.5909G>T	ENSP00000358872.4:p.Cys1970Phe
ENST00000415241.1:c.175G>T
ENST00000420627.5:c.5946G>T	ENSP00000408921.1:n.5946G>T
ENST00000422373.5:c.5966G>T	ENSP00000416926.1:p.Cys1989Phe
ENST00000438732.2:c.664G>T
ENST00000466325.1:n.129G>T
ENST00000490936.5:n.1979G>T
ENST00000610817.4:c.5844+65G>T	ENSP00000480593.1:n.5844+65G>T
NM_001110556.1:c.5990G>T	NP_001104026.1:p.Cys1997Phe
NM_001456.3:c.5966G>T	NP_001447.2:p.Cys1989Phe
XM_011531127.1:c.5894G>T	XP_011529429.1:p.Cys1965Phe
XM_011531128.1:c.5870G>T	XP_011529430.1:p.Cys1957Phe
XM_011531129.1:c.5816G>T	XP_011529431.1:p.Cys1939Phe
XM_011531130.1:c.5792G>T	XP_011529432.1:p.Cys1931Phe
XM_011531131.1:c.5789G>T	XP_011529433.1:p.Cys1930Phe
NM_001110556.2:c.5990G>T MANE Select	NP_001104026.1:p.Cys1997Phe
NM_001456.4:c.5966G>T	NP_001447.2:p.Cys1989Phe