Canonical Allele Identifier: CA2580101848

Gene: FLNA

Linked Data

• ClinVar Variation Id: 2109071
• ClinVar RCV Id: RCV003019911
• gnomAD v4: X-154349041-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154349041G>C , CM000685.2:g.154349041G>C	GRCh38
NC_000023.10:g.153577409G>C , CM000685.1:g.153577409G>C	GRCh37
NC_000023.9:g.153230603G>C	NCBI36
NG_011506.1:g.30598C>G
NG_011506.2:g.30598C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7733-5C>G	ENSP00000353467.4:n.7733-5C>G
ENST00000369850.10:c.7757-5C>G MANE Select	ENSP00000358866.3:n.7757-5C>G
ENST00000369856.8:c.7676-5C>G	ENSP00000358872.4:n.7676-5C>G
ENST00000422373.6:c.4538-5C>G	ENSP00000416926.2:n.4538-5C>G
ENST00000610817.5:c.7814-5C>G	ENSP00000480593.2:n.7814-5C>G
ENST00000673639.2:c.280-351C>G
ENST00000676696.1:c.8036-5C>G	ENSP00000503392.1:n.8036-5C>G
ENST00000678304.1:n.3475-5C>G
ENST00000344736.8:c.7637-5C>G	ENSP00000358863.3:n.7637-5C>G
ENST00000360319.8:c.7733-5C>G	ENSP00000353467.4:n.7733-5C>G
ENST00000369850.7:c.7757-5C>G	ENSP00000358866.3:n.7757-5C>G
ENST00000369856.7:c.7676-5C>G	ENSP00000358872.4:n.7676-5C>G
ENST00000420627.5:c.7713-5C>G	ENSP00000408921.1:n.7713-5C>G
ENST00000422373.5:c.7733-5C>G	ENSP00000416926.1:n.7733-5C>G
ENST00000462590.1:n.912-5C>G
ENST00000490936.5:n.4986-5C>G
ENST00000498411.1:n.68-211C>G
ENST00000498491.5:n.798-5C>G
ENST00000610817.4:c.6761-5C>G	ENSP00000480593.1:n.6761-5C>G
NM_001110556.1:c.7757-5C>G	NP_001104026.1:n.7757-5C>G
NM_001456.3:c.7733-5C>G	NP_001447.2:n.7733-5C>G
XM_011531127.1:c.7661-5C>G	XP_011529429.1:n.7661-5C>G
XM_011531128.1:c.7637-5C>G	XP_011529430.1:n.7637-5C>G
XM_011531129.1:c.7583-5C>G	XP_011529431.1:n.7583-5C>G
XM_011531130.1:c.7559-5C>G	XP_011529432.1:n.7559-5C>G
XM_011531131.1:c.7556-5C>G	XP_011529433.1:n.7556-5C>G
NM_001110556.2:c.7757-5C>G MANE Select	NP_001104026.1:n.7757-5C>G
NM_001456.4:c.7733-5C>G	NP_001447.2:n.7733-5C>G