Canonical Allele Identifier: CA519706884

Gene: FLNA

Linked Data

• dbSNP Id: rs2067636539
• MyVariant Identifiers: chrX:g.153581694A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353326A>G , CM000685.2:g.154353326A>G	GRCh38
NC_000023.10:g.153581694A>G , CM000685.1:g.153581694A>G	GRCh37
NC_000023.9:g.153234888A>G	NCBI36
NG_011506.1:g.26313T>C
NG_011506.2:g.26313T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5968T>C	ENSP00000353467.4:p.Leu1990=
ENST00000369850.10:c.5992T>C MANE Select	ENSP00000358866.3:p.Leu1998=
ENST00000369856.8:c.5911T>C	ENSP00000358872.4:p.Leu1971=
ENST00000422373.6:c.3161-651T>C	ENSP00000416926.2:n.3161-651T>C
ENST00000610817.5:c.6049T>C	ENSP00000480593.2:n.6049T>C
ENST00000673639.2:c.280-4636T>C
ENST00000676696.1:c.6271T>C	ENSP00000503392.1:n.6271T>C
ENST00000678304.1:n.1171T>C
ENST00000344736.8:c.5872T>C	ENSP00000358863.3:p.Leu1958=
ENST00000360319.8:c.5968T>C	ENSP00000353467.4:p.Leu1990=
ENST00000369850.7:c.5992T>C	ENSP00000358866.3:p.Leu1998=
ENST00000369856.7:c.5911T>C	ENSP00000358872.4:p.Leu1971=
ENST00000415241.1:c.177T>C
ENST00000420627.5:c.5948T>C	ENSP00000408921.1:n.5948T>C
ENST00000422373.5:c.5968T>C	ENSP00000416926.1:p.Leu1990=
ENST00000438732.2:c.666T>C
ENST00000466325.1:n.131T>C
ENST00000490936.5:n.1981T>C
ENST00000610817.4:c.5844+67T>C	ENSP00000480593.1:n.5844+67T>C
NM_001110556.1:c.5992T>C	NP_001104026.1:p.Leu1998=
NM_001456.3:c.5968T>C	NP_001447.2:p.Leu1990=
XM_011531127.1:c.5896T>C	XP_011529429.1:p.Leu1966=
XM_011531128.1:c.5872T>C	XP_011529430.1:p.Leu1958=
XM_011531129.1:c.5818T>C	XP_011529431.1:p.Leu1940=
XM_011531130.1:c.5794T>C	XP_011529432.1:p.Leu1932=
XM_011531131.1:c.5791T>C	XP_011529433.1:p.Leu1931=
NM_001110556.2:c.5992T>C MANE Select	NP_001104026.1:p.Leu1998=
NM_001456.4:c.5968T>C	NP_001447.2:p.Leu1990=