Canonical Allele Identifier: CA10560929

Gene: FLNA

Linked Data

• ClinVar Variation Id: 239016
• ClinVar RCV Id: RCV000226047 ; RCV002315698
• dbSNP Id: rs368187218
• ExAC: X:153590950 C / T
• gnomAD v2: X-153590950-C-T
• gnomAD v4: X-154362582-C-T
• COSMIC: COSM5513920 ; COSM5513921
• MyVariant Identifiers: chrX:g.153590950C>T (hg19) ; chrX:g.154362582C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154362582C>T , CM000685.2:g.154362582C>T	GRCh38
NC_000023.10:g.153590950C>T , CM000685.1:g.153590950C>T	GRCh37
NC_000023.9:g.153244144C>T	NCBI36
NG_011506.1:g.17057G>A
NG_011506.2:g.17057G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.2405-4G>A	ENSP00000353467.4:n.2405-4G>A
ENST00000369850.10:c.2405-4G>A MANE Select	ENSP00000358866.3:n.2405-4G>A
ENST00000369856.8:c.2324-4G>A	ENSP00000358872.4:n.2324-4G>A
ENST00000422373.6:c.2405-4G>A	ENSP00000416926.2:n.2405-4G>A
ENST00000610817.5:c.2462-4G>A	ENSP00000480593.2:n.2462-4G>A
ENST00000673639.2:c.279+2854G>A
ENST00000676696.1:c.2684-4G>A	ENSP00000503392.1:n.2684-4G>A
ENST00000344736.8:c.2405-4G>A	ENSP00000358863.3:n.2405-4G>A
ENST00000360319.8:c.2405-4G>A	ENSP00000353467.4:n.2405-4G>A
ENST00000369850.7:c.2405-4G>A	ENSP00000358866.3:n.2405-4G>A
ENST00000369856.7:c.2324-4G>A	ENSP00000358872.4:n.2324-4G>A
ENST00000420627.5:c.2361-4G>A	ENSP00000408921.1:n.2361-4G>A
ENST00000422373.5:c.2405-4G>A	ENSP00000416926.1:n.2405-4G>A
ENST00000610817.4:c.2324-4G>A	ENSP00000480593.1:n.2324-4G>A
NM_001110556.1:c.2405-4G>A	NP_001104026.1:n.2405-4G>A
NM_001456.3:c.2405-4G>A	NP_001447.2:n.2405-4G>A
XM_011531127.1:c.2405-4G>A	XP_011529429.1:n.2405-4G>A
XM_011531128.1:c.2405-4G>A	XP_011529430.1:n.2405-4G>A
XM_011531129.1:c.2405-4G>A	XP_011529431.1:n.2405-4G>A
XM_011531130.1:c.2405-4G>A	XP_011529432.1:n.2405-4G>A
XM_011531131.1:c.2204-4G>A	XP_011529433.1:n.2204-4G>A
NM_001110556.2:c.2405-4G>A MANE Select	NP_001104026.1:n.2405-4G>A
NM_001456.4:c.2405-4G>A	NP_001447.2:n.2405-4G>A