Canonical Allele Identifier: CA519277559

Gene: FLNA

Linked Data

• ClinVar Variation Id: 1772924
• ClinVar RCV Id: RCV002394580 ; RCV003103704
• COSMIC: COSM4651710 ; COSM4651711
• MyVariant Identifiers: chrX:g.153599470A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371102A>C , CM000685.2:g.154371102A>C	GRCh38
NC_000023.10:g.153599470A>C , CM000685.1:g.153599470A>C	GRCh37
NC_000023.9:g.153252664A>C	NCBI36
NG_008677.1:g.1675A>C , LRG_745:g.1675A>C
NG_011506.1:g.8537T>G
NG_011506.2:g.8537T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.144T>G	ENSP00000353467.4:p.Thr48=
ENST00000369850.10:c.144T>G MANE Select	ENSP00000358866.3:p.Thr48=
ENST00000369856.8:c.63T>G	ENSP00000358872.4:p.Thr21=
ENST00000422373.6:c.144T>G	ENSP00000416926.2:p.Thr48=
ENST00000610817.5:c.144T>G	ENSP00000480593.2:p.Thr48=
ENST00000676696.1:c.144T>G	ENSP00000503392.1:p.Thr48=
ENST00000344736.8:c.144T>G	ENSP00000358863.3:p.Thr48=
ENST00000360319.8:c.144T>G	ENSP00000353467.4:p.Thr48=
ENST00000369850.7:c.144T>G	ENSP00000358866.3:p.Thr48=
ENST00000369856.7:c.63T>G	ENSP00000358872.4:p.Thr21=
ENST00000420627.5:c.102T>G	ENSP00000408921.1:p.Thr34=
ENST00000422373.5:c.144T>G	ENSP00000416926.1:p.Thr48=
ENST00000610817.4:c.63T>G	ENSP00000480593.1:p.Thr21=
NM_001110556.1:c.144T>G	NP_001104026.1:p.Thr48=
NM_001456.3:c.144T>G	NP_001447.2:p.Thr48=
XM_011531127.1:c.144T>G	XP_011529429.1:p.Thr48=
XM_011531128.1:c.144T>G	XP_011529430.1:p.Thr48=
XM_011531129.1:c.144T>G	XP_011529431.1:p.Thr48=
XM_011531130.1:c.144T>G	XP_011529432.1:p.Thr48=
XM_011531131.1:c.144T>G	XP_011529433.1:p.Thr48=
NM_001110556.2:c.144T>G MANE Select	NP_001104026.1:p.Thr48=
NM_001456.4:c.144T>G	NP_001447.2:p.Thr48=