Canonical Allele Identifier: CA873338668

Gene: FLNA

Linked Data

• ClinVar Variation Id: 2137048
• ClinVar RCV Id: RCV003062357
• dbSNP Id: rs1385491716
• MyVariant Identifiers: chrX:g.154353212_154353213insAGGGCATGGCTGTCAGTCAGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353224_154353245dup , CM000685.2:g.154353224_154353245dup	GRCh38
NC_000023.10:g.153581592_153581613dup , CM000685.1:g.153581592_153581613dup	GRCh37
NC_000023.9:g.153234786_153234807dup	NCBI36
NG_011506.1:g.26405_26426dup
NG_011506.2:g.26405_26426dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5999-30_5999-9dup	ENSP00000353467.4:n.5999-30_5999-9dup
ENST00000369850.10:c.6023-30_6023-9dup MANE Select	ENSP00000358866.3:n.6023-30_6023-9dup
ENST00000369856.8:c.5942-30_5942-9dup	ENSP00000358872.4:n.5942-30_5942-9dup
ENST00000422373.6:c.3161-559_3161-538dup	ENSP00000416926.2:n.3161-559_3161-538dup
ENST00000610817.5:c.6080-30_6080-9dup	ENSP00000480593.2:n.6080-30_6080-9dup
ENST00000673639.2:c.280-4544_280-4523dup
ENST00000676696.1:c.6302-30_6302-9dup	ENSP00000503392.1:n.6302-30_6302-9dup
ENST00000678304.1:n.1202-30_1202-9dup
ENST00000344736.8:c.5903-30_5903-9dup	ENSP00000358863.3:n.5903-30_5903-9dup
ENST00000360319.8:c.5999-30_5999-9dup	ENSP00000353467.4:n.5999-30_5999-9dup
ENST00000369850.7:c.6023-30_6023-9dup	ENSP00000358866.3:n.6023-30_6023-9dup
ENST00000369856.7:c.5942-30_5942-9dup	ENSP00000358872.4:n.5942-30_5942-9dup
ENST00000415241.1:c.208-13_216dup
ENST00000420627.5:c.5979-30_5979-9dup	ENSP00000408921.1:n.5979-30_5979-9dup
ENST00000422373.5:c.5999-30_5999-9dup	ENSP00000416926.1:n.5999-30_5999-9dup
ENST00000466325.1:n.162-30_162-9dup
ENST00000490936.5:n.2012-30_2012-9dup
ENST00000610817.4:c.5844+159_5844+180dup	ENSP00000480593.1:n.5844+159_5844+180dup
NM_001110556.1:c.6023-30_6023-9dup	NP_001104026.1:n.6023-30_6023-9dup
NM_001456.3:c.5999-30_5999-9dup	NP_001447.2:n.5999-30_5999-9dup
XM_011531127.1:c.5927-30_5927-9dup	XP_011529429.1:n.5927-30_5927-9dup
XM_011531128.1:c.5903-30_5903-9dup	XP_011529430.1:n.5903-30_5903-9dup
XM_011531129.1:c.5849-30_5849-9dup	XP_011529431.1:n.5849-30_5849-9dup
XM_011531130.1:c.5825-30_5825-9dup	XP_011529432.1:n.5825-30_5825-9dup
XM_011531131.1:c.5822-30_5822-9dup	XP_011529433.1:n.5822-30_5822-9dup
NM_001110556.2:c.6023-30_6023-9dup MANE Select	NP_001104026.1:n.6023-30_6023-9dup
NM_001456.4:c.5999-30_5999-9dup	NP_001447.2:n.5999-30_5999-9dup