Canonical Allele Identifier: CA519709068

Gene: FLNA

Linked Data

• gnomAD v4: X-154362737-G-T
• MyVariant Identifiers: chrX:g.153591105G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154362737G>T , CM000685.2:g.154362737G>T	GRCh38
NC_000023.10:g.153591105G>T , CM000685.1:g.153591105G>T	GRCh37
NC_000023.9:g.153244299G>T	NCBI36
NG_011506.1:g.16902C>A
NG_011506.2:g.16902C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.2328C>A	ENSP00000353467.4:p.Gly776=
ENST00000369850.10:c.2328C>A MANE Select	ENSP00000358866.3:p.Gly776=
ENST00000369856.8:c.2247C>A	ENSP00000358872.4:p.Gly749=
ENST00000422373.6:c.2328C>A	ENSP00000416926.2:p.Gly776=
ENST00000610817.5:c.2385C>A	ENSP00000480593.2:n.2385C>A
ENST00000673639.2:c.279+2699C>A
ENST00000676696.1:c.2607C>A	ENSP00000503392.1:n.2607C>A
ENST00000344736.8:c.2328C>A	ENSP00000358863.3:p.Gly776=
ENST00000360319.8:c.2328C>A	ENSP00000353467.4:p.Gly776=
ENST00000369850.7:c.2328C>A	ENSP00000358866.3:p.Gly776=
ENST00000369856.7:c.2247C>A	ENSP00000358872.4:p.Gly749=
ENST00000420627.5:c.2284C>A	ENSP00000408921.1:n.2284C>A
ENST00000422373.5:c.2328C>A	ENSP00000416926.1:p.Gly776=
ENST00000610817.4:c.2247C>A	ENSP00000480593.1:p.Gly749=
NM_001110556.1:c.2328C>A	NP_001104026.1:p.Gly776=
NM_001456.3:c.2328C>A	NP_001447.2:p.Gly776=
XM_011531127.1:c.2328C>A	XP_011529429.1:p.Gly776=
XM_011531128.1:c.2328C>A	XP_011529430.1:p.Gly776=
XM_011531129.1:c.2328C>A	XP_011529431.1:p.Gly776=
XM_011531130.1:c.2328C>A	XP_011529432.1:p.Gly776=
XM_011531131.1:c.2127C>A	XP_011529433.1:p.Gly709=
NM_001110556.2:c.2328C>A MANE Select	NP_001104026.1:p.Gly776=
NM_001456.4:c.2328C>A	NP_001447.2:p.Gly776=