Canonical Allele Identifier: CA519706894

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581698G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353330G>T , CM000685.2:g.154353330G>T	GRCh38
NC_000023.10:g.153581698G>T , CM000685.1:g.153581698G>T	GRCh37
NC_000023.9:g.153234892G>T	NCBI36
NG_011506.1:g.26309C>A
NG_011506.2:g.26309C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5964C>A	ENSP00000353467.4:p.Pro1988=
ENST00000369850.10:c.5988C>A MANE Select	ENSP00000358866.3:p.Pro1996=
ENST00000369856.8:c.5907C>A	ENSP00000358872.4:p.Pro1969=
ENST00000422373.6:c.3161-655C>A	ENSP00000416926.2:n.3161-655C>A
ENST00000610817.5:c.6045C>A	ENSP00000480593.2:n.6045C>A
ENST00000673639.2:c.280-4640C>A
ENST00000676696.1:c.6267C>A	ENSP00000503392.1:n.6267C>A
ENST00000678304.1:n.1167C>A
ENST00000344736.8:c.5868C>A	ENSP00000358863.3:p.Pro1956=
ENST00000360319.8:c.5964C>A	ENSP00000353467.4:p.Pro1988=
ENST00000369850.7:c.5988C>A	ENSP00000358866.3:p.Pro1996=
ENST00000369856.7:c.5907C>A	ENSP00000358872.4:p.Pro1969=
ENST00000415241.1:c.173C>A
ENST00000420627.5:c.5944C>A	ENSP00000408921.1:n.5944C>A
ENST00000422373.5:c.5964C>A	ENSP00000416926.1:p.Pro1988=
ENST00000438732.2:c.662C>A
ENST00000466325.1:n.127C>A
ENST00000490936.5:n.1977C>A
ENST00000610817.4:c.5844+63C>A	ENSP00000480593.1:n.5844+63C>A
NM_001110556.1:c.5988C>A	NP_001104026.1:p.Pro1996=
NM_001456.3:c.5964C>A	NP_001447.2:p.Pro1988=
XM_011531127.1:c.5892C>A	XP_011529429.1:p.Pro1964=
XM_011531128.1:c.5868C>A	XP_011529430.1:p.Pro1956=
XM_011531129.1:c.5814C>A	XP_011529431.1:p.Pro1938=
XM_011531130.1:c.5790C>A	XP_011529432.1:p.Pro1930=
XM_011531131.1:c.5787C>A	XP_011529433.1:p.Pro1929=
NM_001110556.2:c.5988C>A MANE Select	NP_001104026.1:p.Pro1996=
NM_001456.4:c.5964C>A	NP_001447.2:p.Pro1988=