Canonical Allele Identifier: CA415197400

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581717G>A (hg19) ; chrX:g.154353349G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353349G>A , CM000685.2:g.154353349G>A	GRCh38
NC_000023.10:g.153581717G>A , CM000685.1:g.153581717G>A	GRCh37
NC_000023.9:g.153234911G>A	NCBI36
NG_011506.1:g.26290C>T
NG_011506.2:g.26290C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5945C>T	ENSP00000353467.4:p.Pro1982Leu
ENST00000369850.10:c.5969C>T MANE Select	ENSP00000358866.3:p.Pro1990Leu
ENST00000369856.8:c.5888C>T	ENSP00000358872.4:p.Pro1963Leu
ENST00000422373.6:c.3161-674C>T	ENSP00000416926.2:n.3161-674C>T
ENST00000610817.5:c.6026C>T	ENSP00000480593.2:n.6026C>T
ENST00000673639.2:c.280-4659C>T
ENST00000676696.1:c.6248C>T	ENSP00000503392.1:n.6248C>T
ENST00000678304.1:n.1148C>T
ENST00000344736.8:c.5849C>T	ENSP00000358863.3:p.Pro1950Leu
ENST00000360319.8:c.5945C>T	ENSP00000353467.4:p.Pro1982Leu
ENST00000369850.7:c.5969C>T	ENSP00000358866.3:p.Pro1990Leu
ENST00000369856.7:c.5888C>T	ENSP00000358872.4:p.Pro1963Leu
ENST00000415241.1:c.154C>T
ENST00000420627.5:c.5925C>T	ENSP00000408921.1:n.5925C>T
ENST00000422373.5:c.5945C>T	ENSP00000416926.1:p.Pro1982Leu
ENST00000438732.2:c.643C>T
ENST00000466325.1:n.108C>T
ENST00000490936.5:n.1958C>T
ENST00000610817.4:c.5844+44C>T	ENSP00000480593.1:n.5844+44C>T
NM_001110556.1:c.5969C>T	NP_001104026.1:p.Pro1990Leu
NM_001456.3:c.5945C>T	NP_001447.2:p.Pro1982Leu
XM_011531127.1:c.5873C>T	XP_011529429.1:p.Pro1958Leu
XM_011531128.1:c.5849C>T	XP_011529430.1:p.Pro1950Leu
XM_011531129.1:c.5795C>T	XP_011529431.1:p.Pro1932Leu
XM_011531130.1:c.5771C>T	XP_011529432.1:p.Pro1924Leu
XM_011531131.1:c.5768C>T	XP_011529433.1:p.Pro1923Leu
NM_001110556.2:c.5969C>T MANE Select	NP_001104026.1:p.Pro1990Leu
NM_001456.4:c.5945C>T	NP_001447.2:p.Pro1982Leu