Canonical Allele Identifier: CA415196023

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581483C>T (hg19) ; chrX:g.154353115C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353115C>T , CM000685.2:g.154353115C>T	GRCh38
NC_000023.10:g.153581483C>T , CM000685.1:g.153581483C>T	GRCh37
NC_000023.9:g.153234677C>T	NCBI36
NG_011506.1:g.26524G>A
NG_011506.2:g.26524G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6088G>A	ENSP00000353467.4:p.Val2030Met
ENST00000369850.10:c.6112G>A MANE Select	ENSP00000358866.3:p.Val2038Met
ENST00000369856.8:c.6031G>A	ENSP00000358872.4:p.Val2011Met
ENST00000422373.6:c.3161-440G>A	ENSP00000416926.2:n.3161-440G>A
ENST00000610817.5:c.6169G>A	ENSP00000480593.2:n.6169G>A
ENST00000673639.2:c.280-4425G>A
ENST00000676696.1:c.6391G>A	ENSP00000503392.1:n.6391G>A
ENST00000678304.1:n.1291G>A
ENST00000344736.8:c.5992G>A	ENSP00000358863.3:p.Val1998Met
ENST00000360319.8:c.6088G>A	ENSP00000353467.4:p.Val2030Met
ENST00000369850.7:c.6112G>A	ENSP00000358866.3:p.Val2038Met
ENST00000369856.7:c.6031G>A	ENSP00000358872.4:p.Val2011Met
ENST00000415241.1:c.314G>A
ENST00000420627.5:c.6068G>A	ENSP00000408921.1:n.6068G>A
ENST00000422373.5:c.6088G>A	ENSP00000416926.1:p.Val2030Met
ENST00000444578.1:c.55G>A	ENSP00000397824.1:p.Val19Met
ENST00000466325.1:n.251G>A
ENST00000490936.5:n.2101G>A
ENST00000610817.4:c.5844+278G>A	ENSP00000480593.1:n.5844+278G>A
NM_001110556.1:c.6112G>A	NP_001104026.1:p.Val2038Met
NM_001456.3:c.6088G>A	NP_001447.2:p.Val2030Met
XM_011531127.1:c.6016G>A	XP_011529429.1:p.Val2006Met
XM_011531128.1:c.5992G>A	XP_011529430.1:p.Val1998Met
XM_011531129.1:c.5938G>A	XP_011529431.1:p.Val1980Met
XM_011531130.1:c.5914G>A	XP_011529432.1:p.Val1972Met
XM_011531131.1:c.5911G>A	XP_011529433.1:p.Val1971Met
NM_001110556.2:c.6112G>A MANE Select	NP_001104026.1:p.Val2038Met
NM_001456.4:c.6088G>A	NP_001447.2:p.Val2030Met