Canonical Allele Identifier: CA519706874

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581689C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353321C>G , CM000685.2:g.154353321C>G	GRCh38
NC_000023.10:g.153581689C>G , CM000685.1:g.153581689C>G	GRCh37
NC_000023.9:g.153234883C>G	NCBI36
NG_011506.1:g.26318G>C
NG_011506.2:g.26318G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5973G>C	ENSP00000353467.4:p.Leu1991=
ENST00000369850.10:c.5997G>C MANE Select	ENSP00000358866.3:p.Leu1999=
ENST00000369856.8:c.5916G>C	ENSP00000358872.4:p.Leu1972=
ENST00000422373.6:c.3161-646G>C	ENSP00000416926.2:n.3161-646G>C
ENST00000610817.5:c.6054G>C	ENSP00000480593.2:n.6054G>C
ENST00000673639.2:c.280-4631G>C
ENST00000676696.1:c.6276G>C	ENSP00000503392.1:n.6276G>C
ENST00000678304.1:n.1176G>C
ENST00000344736.8:c.5877G>C	ENSP00000358863.3:p.Leu1959=
ENST00000360319.8:c.5973G>C	ENSP00000353467.4:p.Leu1991=
ENST00000369850.7:c.5997G>C	ENSP00000358866.3:p.Leu1999=
ENST00000369856.7:c.5916G>C	ENSP00000358872.4:p.Leu1972=
ENST00000415241.1:c.182G>C
ENST00000420627.5:c.5953G>C	ENSP00000408921.1:n.5953G>C
ENST00000422373.5:c.5973G>C	ENSP00000416926.1:p.Leu1991=
ENST00000438732.2:c.671G>C
ENST00000466325.1:n.136G>C
ENST00000490936.5:n.1986G>C
ENST00000610817.4:c.5844+72G>C	ENSP00000480593.1:n.5844+72G>C
NM_001110556.1:c.5997G>C	NP_001104026.1:p.Leu1999=
NM_001456.3:c.5973G>C	NP_001447.2:p.Leu1991=
XM_011531127.1:c.5901G>C	XP_011529429.1:p.Leu1967=
XM_011531128.1:c.5877G>C	XP_011529430.1:p.Leu1959=
XM_011531129.1:c.5823G>C	XP_011529431.1:p.Leu1941=
XM_011531130.1:c.5799G>C	XP_011529432.1:p.Leu1933=
XM_011531131.1:c.5796G>C	XP_011529433.1:p.Leu1932=
NM_001110556.2:c.5997G>C MANE Select	NP_001104026.1:p.Leu1999=
NM_001456.4:c.5973G>C	NP_001447.2:p.Leu1991=