Canonical Allele Identifier: CA415197462

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581723A>T (hg19) ; chrX:g.154353355A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353355A>T , CM000685.2:g.154353355A>T	GRCh38
NC_000023.10:g.153581723A>T , CM000685.1:g.153581723A>T	GRCh37
NC_000023.9:g.153234917A>T	NCBI36
NG_011506.1:g.26284T>A
NG_011506.2:g.26284T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5939T>A	ENSP00000353467.4:p.Val1980Asp
ENST00000369850.10:c.5963T>A MANE Select	ENSP00000358866.3:p.Val1988Asp
ENST00000369856.8:c.5882T>A	ENSP00000358872.4:p.Val1961Asp
ENST00000422373.6:c.3161-680T>A	ENSP00000416926.2:n.3161-680T>A
ENST00000610817.5:c.6020T>A	ENSP00000480593.2:n.6020T>A
ENST00000673639.2:c.280-4665T>A
ENST00000676696.1:c.6242T>A	ENSP00000503392.1:n.6242T>A
ENST00000678304.1:n.1142T>A
ENST00000344736.8:c.5843T>A	ENSP00000358863.3:p.Val1948Asp
ENST00000360319.8:c.5939T>A	ENSP00000353467.4:p.Val1980Asp
ENST00000369850.7:c.5963T>A	ENSP00000358866.3:p.Val1988Asp
ENST00000369856.7:c.5882T>A	ENSP00000358872.4:p.Val1961Asp
ENST00000415241.1:c.148T>A
ENST00000420627.5:c.5919T>A	ENSP00000408921.1:n.5919T>A
ENST00000422373.5:c.5939T>A	ENSP00000416926.1:p.Val1980Asp
ENST00000438732.2:c.637T>A
ENST00000466325.1:n.102T>A
ENST00000490936.5:n.1952T>A
ENST00000610817.4:c.5844+38T>A	ENSP00000480593.1:n.5844+38T>A
NM_001110556.1:c.5963T>A	NP_001104026.1:p.Val1988Asp
NM_001456.3:c.5939T>A	NP_001447.2:p.Val1980Asp
XM_011531127.1:c.5867T>A	XP_011529429.1:p.Val1956Asp
XM_011531128.1:c.5843T>A	XP_011529430.1:p.Val1948Asp
XM_011531129.1:c.5789T>A	XP_011529431.1:p.Val1930Asp
XM_011531130.1:c.5765T>A	XP_011529432.1:p.Val1922Asp
XM_011531131.1:c.5762T>A	XP_011529433.1:p.Val1921Asp
NM_001110556.2:c.5963T>A MANE Select	NP_001104026.1:p.Val1988Asp
NM_001456.4:c.5939T>A	NP_001447.2:p.Val1980Asp