Canonical Allele Identifier: CA2695083165

Gene: FLNA

Linked Data

• gnomAD v4: X-154368123-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154368125dup , CM000685.2:g.154368125dup	GRCh38
NC_000023.10:g.153596493dup , CM000685.1:g.153596493dup	GRCh37
NC_000023.9:g.153249687dup	NCBI36
NG_011506.1:g.11515dup
NG_011506.2:g.11515dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.374-34dup	ENSP00000353467.4:n.374-34dup
ENST00000369850.10:c.374-34dup MANE Select	ENSP00000358866.3:n.374-34dup
ENST00000369856.8:c.293-34dup	ENSP00000358872.4:n.293-34dup
ENST00000422373.6:c.374-34dup	ENSP00000416926.2:n.374-34dup
ENST00000610817.5:c.374-34dup	ENSP00000480593.2:n.374-34dup
ENST00000676696.1:c.374-34dup	ENSP00000503392.1:n.374-34dup
ENST00000344736.8:c.374-34dup	ENSP00000358863.3:n.374-34dup
ENST00000360319.8:c.374-34dup	ENSP00000353467.4:n.374-34dup
ENST00000369850.7:c.374-34dup	ENSP00000358866.3:n.374-34dup
ENST00000369856.7:c.293-34dup	ENSP00000358872.4:n.293-34dup
ENST00000420627.5:c.332-34dup	ENSP00000408921.1:n.332-34dup
ENST00000422373.5:c.374-34dup	ENSP00000416926.1:n.374-34dup
ENST00000610817.4:c.293-34dup	ENSP00000480593.1:n.293-34dup
NM_001110556.1:c.374-34dup	NP_001104026.1:n.374-34dup
NM_001456.3:c.374-34dup	NP_001447.2:n.374-34dup
XM_011531127.1:c.374-34dup	XP_011529429.1:n.374-34dup
XM_011531128.1:c.374-34dup	XP_011529430.1:n.374-34dup
XM_011531129.1:c.374-34dup	XP_011529431.1:n.374-34dup
XM_011531130.1:c.374-34dup	XP_011529432.1:n.374-34dup
XM_011531131.1:c.374-34dup	XP_011529433.1:n.374-34dup
NM_001110556.2:c.374-34dup MANE Select	NP_001104026.1:n.374-34dup
NM_001456.4:c.374-34dup	NP_001447.2:n.374-34dup