Canonical Allele Identifier: CA645290167

Gene: FLNA

Linked Data

• ClinVar Variation Id: 1899176
• ClinVar RCV Id: RCV002570245
• dbSNP Id: rs1202642295
• gnomAD v2: X-153581301-T-A
• MyVariant Identifiers: chrX:g.153581301T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352933T>A , CM000685.2:g.154352933T>A	GRCh38
NC_000023.10:g.153581301T>A , CM000685.1:g.153581301T>A	GRCh37
NC_000023.9:g.153234495T>A	NCBI36
NG_011506.1:g.26706A>T
NG_011506.2:g.26706A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6203-9A>T	ENSP00000353467.4:n.6203-9A>T
ENST00000369850.10:c.6227-9A>T MANE Select	ENSP00000358866.3:n.6227-9A>T
ENST00000369856.8:c.6146-9A>T	ENSP00000358872.4:n.6146-9A>T
ENST00000422373.6:c.3161-258A>T	ENSP00000416926.2:n.3161-258A>T
ENST00000610817.5:c.6284-9A>T	ENSP00000480593.2:n.6284-9A>T
ENST00000673639.2:c.280-4243A>T
ENST00000676696.1:c.6506-9A>T	ENSP00000503392.1:n.6506-9A>T
ENST00000678304.1:n.1406-9A>T
ENST00000344736.8:c.6107-9A>T	ENSP00000358863.3:n.6107-9A>T
ENST00000360319.8:c.6203-9A>T	ENSP00000353467.4:n.6203-9A>T
ENST00000369850.7:c.6227-9A>T	ENSP00000358866.3:n.6227-9A>T
ENST00000369856.7:c.6146-9A>T	ENSP00000358872.4:n.6146-9A>T
ENST00000415241.1:c.429-9A>T
ENST00000420627.5:c.6183-9A>T	ENSP00000408921.1:n.6183-9A>T
ENST00000422373.5:c.6203-9A>T	ENSP00000416926.1:n.6203-9A>T
ENST00000444578.1:c.170-9A>T	ENSP00000397824.1:n.170-9A>T
ENST00000466325.1:n.433A>T
ENST00000490936.5:n.2216-9A>T
ENST00000610817.4:c.5844+460A>T	ENSP00000480593.1:n.5844+460A>T
NM_001110556.1:c.6227-9A>T	NP_001104026.1:n.6227-9A>T
NM_001456.3:c.6203-9A>T	NP_001447.2:n.6203-9A>T
XM_011531127.1:c.6131-9A>T	XP_011529429.1:n.6131-9A>T
XM_011531128.1:c.6107-9A>T	XP_011529430.1:n.6107-9A>T
XM_011531129.1:c.6053-9A>T	XP_011529431.1:n.6053-9A>T
XM_011531130.1:c.6029-9A>T	XP_011529432.1:n.6029-9A>T
XM_011531131.1:c.6026-9A>T	XP_011529433.1:n.6026-9A>T
NM_001110556.2:c.6227-9A>T MANE Select	NP_001104026.1:n.6227-9A>T
NM_001456.4:c.6203-9A>T	NP_001447.2:n.6203-9A>T