Canonical Allele Identifier: CA10561445

Gene: FLNA

Linked Data

• ClinVar Variation Id: 1734370
• ClinVar RCV Id: RCV002349168
• dbSNP Id: rs782616358
• ExAC: X:153599242 G / A
• gnomAD v2: X-153599242-G-A
• gnomAD v4: X-154370874-G-A
• MyVariant Identifiers: chrX:g.153599242G>A (hg19) ; chrX:g.154370874G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154370874G>A , CM000685.2:g.154370874G>A	GRCh38
NC_000023.10:g.153599242G>A , CM000685.1:g.153599242G>A	GRCh37
NC_000023.9:g.153252436G>A	NCBI36
NG_008677.1:g.1447G>A , LRG_745:g.1447G>A
NG_011506.1:g.8765C>T
NG_011506.2:g.8765C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.372C>T	ENSP00000353467.4:p.Ile124=
ENST00000369850.10:c.372C>T MANE Select	ENSP00000358866.3:p.Ile124=
ENST00000369856.8:c.291C>T	ENSP00000358872.4:p.Ile97=
ENST00000422373.6:c.372C>T	ENSP00000416926.2:p.Ile124=
ENST00000610817.5:c.372C>T	ENSP00000480593.2:p.Ile124=
ENST00000676696.1:c.372C>T	ENSP00000503392.1:p.Ile124=
ENST00000344736.8:c.372C>T	ENSP00000358863.3:p.Ile124=
ENST00000360319.8:c.372C>T	ENSP00000353467.4:p.Ile124=
ENST00000369850.7:c.372C>T	ENSP00000358866.3:p.Ile124=
ENST00000369856.7:c.291C>T	ENSP00000358872.4:p.Ile97=
ENST00000420627.5:c.330C>T	ENSP00000408921.1:p.Ile110=
ENST00000422373.5:c.372C>T	ENSP00000416926.1:p.Ile124=
ENST00000610817.4:c.291C>T	ENSP00000480593.1:p.Ile97=
NM_001110556.1:c.372C>T	NP_001104026.1:p.Ile124=
NM_001456.3:c.372C>T	NP_001447.2:p.Ile124=
XM_011531127.1:c.372C>T	XP_011529429.1:p.Ile124=
XM_011531128.1:c.372C>T	XP_011529430.1:p.Ile124=
XM_011531129.1:c.372C>T	XP_011529431.1:p.Ile124=
XM_011531130.1:c.372C>T	XP_011529432.1:p.Ile124=
XM_011531131.1:c.372C>T	XP_011529433.1:p.Ile124=
NM_001110556.2:c.372C>T MANE Select	NP_001104026.1:p.Ile124=
NM_001456.4:c.372C>T	NP_001447.2:p.Ile124=