Canonical Allele Identifier: CA415197164

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581692C>A (hg19) ; chrX:g.154353324C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353324C>A , CM000685.2:g.154353324C>A	GRCh38
NC_000023.10:g.153581692C>A , CM000685.1:g.153581692C>A	GRCh37
NC_000023.9:g.153234886C>A	NCBI36
NG_011506.1:g.26315G>T
NG_011506.2:g.26315G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5970G>T	ENSP00000353467.4:p.Leu1990Phe
ENST00000369850.10:c.5994G>T MANE Select	ENSP00000358866.3:p.Leu1998Phe
ENST00000369856.8:c.5913G>T	ENSP00000358872.4:p.Leu1971Phe
ENST00000422373.6:c.3161-649G>T	ENSP00000416926.2:n.3161-649G>T
ENST00000610817.5:c.6051G>T	ENSP00000480593.2:n.6051G>T
ENST00000673639.2:c.280-4634G>T
ENST00000676696.1:c.6273G>T	ENSP00000503392.1:n.6273G>T
ENST00000678304.1:n.1173G>T
ENST00000344736.8:c.5874G>T	ENSP00000358863.3:p.Leu1958Phe
ENST00000360319.8:c.5970G>T	ENSP00000353467.4:p.Leu1990Phe
ENST00000369850.7:c.5994G>T	ENSP00000358866.3:p.Leu1998Phe
ENST00000369856.7:c.5913G>T	ENSP00000358872.4:p.Leu1971Phe
ENST00000415241.1:c.179G>T
ENST00000420627.5:c.5950G>T	ENSP00000408921.1:n.5950G>T
ENST00000422373.5:c.5970G>T	ENSP00000416926.1:p.Leu1990Phe
ENST00000438732.2:c.668G>T
ENST00000466325.1:n.133G>T
ENST00000490936.5:n.1983G>T
ENST00000610817.4:c.5844+69G>T	ENSP00000480593.1:n.5844+69G>T
NM_001110556.1:c.5994G>T	NP_001104026.1:p.Leu1998Phe
NM_001456.3:c.5970G>T	NP_001447.2:p.Leu1990Phe
XM_011531127.1:c.5898G>T	XP_011529429.1:p.Leu1966Phe
XM_011531128.1:c.5874G>T	XP_011529430.1:p.Leu1958Phe
XM_011531129.1:c.5820G>T	XP_011529431.1:p.Leu1940Phe
XM_011531130.1:c.5796G>T	XP_011529432.1:p.Leu1932Phe
XM_011531131.1:c.5793G>T	XP_011529433.1:p.Leu1931Phe
NM_001110556.2:c.5994G>T MANE Select	NP_001104026.1:p.Leu1998Phe
NM_001456.4:c.5970G>T	NP_001447.2:p.Leu1990Phe