Canonical Allele Identifier: CA519277307

Gene: FLNA

Linked Data

• ClinVar Variation Id: 793677
• ClinVar RCV Id: RCV001479196
• dbSNP Id: rs1603363881
• gnomAD v4: X-154370901-G-A
• MyVariant Identifiers: chrX:g.153599269G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154370901G>A , CM000685.2:g.154370901G>A	GRCh38
NC_000023.10:g.153599269G>A , CM000685.1:g.153599269G>A	GRCh37
NC_000023.9:g.153252463G>A	NCBI36
NG_008677.1:g.1474G>A , LRG_745:g.1474G>A
NG_011506.1:g.8738C>T
NG_011506.2:g.8738C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.345C>T	ENSP00000353467.4:p.Asp115=
ENST00000369850.10:c.345C>T MANE Select	ENSP00000358866.3:p.Asp115=
ENST00000369856.8:c.264C>T	ENSP00000358872.4:p.Asp88=
ENST00000422373.6:c.345C>T	ENSP00000416926.2:p.Asp115=
ENST00000610817.5:c.345C>T	ENSP00000480593.2:p.Asp115=
ENST00000676696.1:c.345C>T	ENSP00000503392.1:p.Asp115=
ENST00000344736.8:c.345C>T	ENSP00000358863.3:p.Asp115=
ENST00000360319.8:c.345C>T	ENSP00000353467.4:p.Asp115=
ENST00000369850.7:c.345C>T	ENSP00000358866.3:p.Asp115=
ENST00000369856.7:c.264C>T	ENSP00000358872.4:p.Asp88=
ENST00000420627.5:c.303C>T	ENSP00000408921.1:p.Asp101=
ENST00000422373.5:c.345C>T	ENSP00000416926.1:p.Asp115=
ENST00000610817.4:c.264C>T	ENSP00000480593.1:p.Asp88=
NM_001110556.1:c.345C>T	NP_001104026.1:p.Asp115=
NM_001456.3:c.345C>T	NP_001447.2:p.Asp115=
XM_011531127.1:c.345C>T	XP_011529429.1:p.Asp115=
XM_011531128.1:c.345C>T	XP_011529430.1:p.Asp115=
XM_011531129.1:c.345C>T	XP_011529431.1:p.Asp115=
XM_011531130.1:c.345C>T	XP_011529432.1:p.Asp115=
XM_011531131.1:c.345C>T	XP_011529433.1:p.Asp115=
NM_001110556.2:c.345C>T MANE Select	NP_001104026.1:p.Asp115=
NM_001456.4:c.345C>T	NP_001447.2:p.Asp115=