Canonical Allele Identifier: CA2695112068

Gene: FLNA

Linked Data

• gnomAD v4: X-154353211-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353211A>C , CM000685.2:g.154353211A>C	GRCh38
NC_000023.10:g.153581579A>C , CM000685.1:g.153581579A>C	GRCh37
NC_000023.9:g.153234773A>C	NCBI36
NG_011506.1:g.26428T>G
NG_011506.2:g.26428T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5999-7T>G	ENSP00000353467.4:n.5999-7T>G
ENST00000369850.10:c.6023-7T>G MANE Select	ENSP00000358866.3:n.6023-7T>G
ENST00000369856.8:c.5942-7T>G	ENSP00000358872.4:n.5942-7T>G
ENST00000422373.6:c.3161-536T>G	ENSP00000416926.2:n.3161-536T>G
ENST00000610817.5:c.6080-7T>G	ENSP00000480593.2:n.6080-7T>G
ENST00000673639.2:c.280-4521T>G
ENST00000676696.1:c.6302-7T>G	ENSP00000503392.1:n.6302-7T>G
ENST00000678304.1:n.1202-7T>G
ENST00000344736.8:c.5903-7T>G	ENSP00000358863.3:n.5903-7T>G
ENST00000360319.8:c.5999-7T>G	ENSP00000353467.4:n.5999-7T>G
ENST00000369850.7:c.6023-7T>G	ENSP00000358866.3:n.6023-7T>G
ENST00000369856.7:c.5942-7T>G	ENSP00000358872.4:n.5942-7T>G
ENST00000415241.1:c.218T>G
ENST00000420627.5:c.5979-7T>G	ENSP00000408921.1:n.5979-7T>G
ENST00000422373.5:c.5999-7T>G	ENSP00000416926.1:n.5999-7T>G
ENST00000466325.1:n.162-7T>G
ENST00000490936.5:n.2012-7T>G
ENST00000610817.4:c.5844+182T>G	ENSP00000480593.1:n.5844+182T>G
NM_001110556.1:c.6023-7T>G	NP_001104026.1:n.6023-7T>G
NM_001456.3:c.5999-7T>G	NP_001447.2:n.5999-7T>G
XM_011531127.1:c.5927-7T>G	XP_011529429.1:n.5927-7T>G
XM_011531128.1:c.5903-7T>G	XP_011529430.1:n.5903-7T>G
XM_011531129.1:c.5849-7T>G	XP_011529431.1:n.5849-7T>G
XM_011531130.1:c.5825-7T>G	XP_011529432.1:n.5825-7T>G
XM_011531131.1:c.5822-7T>G	XP_011529433.1:n.5822-7T>G
NM_001110556.2:c.6023-7T>G MANE Select	NP_001104026.1:n.6023-7T>G
NM_001456.4:c.5999-7T>G	NP_001447.2:n.5999-7T>G