Canonical Allele Identifier: CA10560162

Gene: FLNA

Linked Data

• dbSNP Id: rs782495475
• ExAC: X:153581480 TCAC / T
• gnomAD v2: X-153581480-TCAC-T
• gnomAD v4: X-154353112-TCAC-T
• MyVariant Identifiers: chrX:g.153581481_153581483del (hg19) ; chrX:g.154353113_154353115del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353117_154353119del , CM000685.2:g.154353117_154353119del	GRCh38
NC_000023.10:g.153581485_153581487del , CM000685.1:g.153581485_153581487del	GRCh37
NC_000023.9:g.153234679_153234681del	NCBI36
NG_011506.1:g.26524_26526del
NG_011506.2:g.26524_26526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6088_6090del	ENSP00000353467.4:p.Val2030del
ENST00000369850.10:c.6112_6114del MANE Select	ENSP00000358866.3:p.Val2038del
ENST00000369856.8:c.6031_6033del	ENSP00000358872.4:p.Val2011del
ENST00000422373.6:c.3161-440_3161-438del	ENSP00000416926.2:n.3161-440_3161-438del
ENST00000610817.5:c.6169_6171del	ENSP00000480593.2:n.6169_6171del
ENST00000673639.2:c.280-4425_280-4423del
ENST00000676696.1:c.6391_6393del	ENSP00000503392.1:n.6391_6393del
ENST00000678304.1:n.1291_1293del
ENST00000344736.8:c.5992_5994del	ENSP00000358863.3:p.Val1998del
ENST00000360319.8:c.6088_6090del	ENSP00000353467.4:p.Val2030del
ENST00000369850.7:c.6112_6114del	ENSP00000358866.3:p.Val2038del
ENST00000369856.7:c.6031_6033del	ENSP00000358872.4:p.Val2011del
ENST00000415241.1:c.314_316del
ENST00000420627.5:c.6068_6070del	ENSP00000408921.1:n.6068_6070del
ENST00000422373.5:c.6088_6090del	ENSP00000416926.1:p.Val2030del
ENST00000444578.1:c.55_57del	ENSP00000397824.1:p.Val19del
ENST00000466325.1:n.251_253del
ENST00000490936.5:n.2101_2103del
ENST00000610817.4:c.5844+278_5844+280del	ENSP00000480593.1:n.5844+278_5844+280del
NM_001110556.1:c.6112_6114del	NP_001104026.1:p.Val2038del
NM_001456.3:c.6088_6090del	NP_001447.2:p.Val2030del
XM_011531127.1:c.6016_6018del	XP_011529429.1:p.Val2006del
XM_011531128.1:c.5992_5994del	XP_011529430.1:p.Val1998del
XM_011531129.1:c.5938_5940del	XP_011529431.1:p.Val1980del
XM_011531130.1:c.5914_5916del	XP_011529432.1:p.Val1972del
XM_011531131.1:c.5911_5913del	XP_011529433.1:p.Val1971del
NM_001110556.2:c.6112_6114del MANE Select	NP_001104026.1:p.Val2038del
NM_001456.4:c.6088_6090del	NP_001447.2:p.Val2030del