Canonical Allele Identifier: CA415197190

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581694A>C (hg19) ; chrX:g.154353326A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5968T>G	ENSP00000353467.4:p.Leu1990Val
ENST00000369850.10:c.5992T>G MANE Select	ENSP00000358866.3:p.Leu1998Val
ENST00000369856.8:c.5911T>G	ENSP00000358872.4:p.Leu1971Val
ENST00000422373.6:c.3161-651T>G	ENSP00000416926.2:n.3161-651T>G
ENST00000610817.5:c.6049T>G	ENSP00000480593.2:n.6049T>G
ENST00000673639.2:c.280-4636T>G
ENST00000676696.1:c.6271T>G	ENSP00000503392.1:n.6271T>G
ENST00000678304.1:n.1171T>G
ENST00000344736.8:c.5872T>G	ENSP00000358863.3:p.Leu1958Val
ENST00000360319.8:c.5968T>G	ENSP00000353467.4:p.Leu1990Val
ENST00000369850.7:c.5992T>G	ENSP00000358866.3:p.Leu1998Val
ENST00000369856.7:c.5911T>G	ENSP00000358872.4:p.Leu1971Val
ENST00000415241.1:c.177T>G
ENST00000420627.5:c.5948T>G	ENSP00000408921.1:n.5948T>G
ENST00000422373.5:c.5968T>G	ENSP00000416926.1:p.Leu1990Val
ENST00000438732.2:c.666T>G
ENST00000466325.1:n.131T>G
ENST00000490936.5:n.1981T>G
ENST00000610817.4:c.5844+67T>G	ENSP00000480593.1:n.5844+67T>G
NM_001110556.1:c.5992T>G	NP_001104026.1:p.Leu1998Val
NM_001456.3:c.5968T>G	NP_001447.2:p.Leu1990Val
XM_011531127.1:c.5896T>G	XP_011529429.1:p.Leu1966Val
XM_011531128.1:c.5872T>G	XP_011529430.1:p.Leu1958Val
XM_011531129.1:c.5818T>G	XP_011529431.1:p.Leu1940Val
XM_011531130.1:c.5794T>G	XP_011529432.1:p.Leu1932Val
XM_011531131.1:c.5791T>G	XP_011529433.1:p.Leu1931Val
NM_001110556.2:c.5992T>G MANE Select	NP_001104026.1:p.Leu1998Val
NM_001456.4:c.5968T>G	NP_001447.2:p.Leu1990Val