Canonical Allele Identifier: CA415196952

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581673C>A (hg19) ; chrX:g.154353305C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353305C>A , CM000685.2:g.154353305C>A	GRCh38
NC_000023.10:g.153581673C>A , CM000685.1:g.153581673C>A	GRCh37
NC_000023.9:g.153234867C>A	NCBI36
NG_011506.1:g.26334G>T
NG_011506.2:g.26334G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5989G>T	ENSP00000353467.4:p.Gly1997Cys
ENST00000369850.10:c.6013G>T MANE Select	ENSP00000358866.3:p.Gly2005Cys
ENST00000369856.8:c.5932G>T	ENSP00000358872.4:p.Gly1978Cys
ENST00000422373.6:c.3161-630G>T	ENSP00000416926.2:n.3161-630G>T
ENST00000610817.5:c.6070G>T	ENSP00000480593.2:n.6070G>T
ENST00000673639.2:c.280-4615G>T
ENST00000676696.1:c.6292G>T	ENSP00000503392.1:n.6292G>T
ENST00000678304.1:n.1192G>T
ENST00000344736.8:c.5893G>T	ENSP00000358863.3:p.Gly1965Cys
ENST00000360319.8:c.5989G>T	ENSP00000353467.4:p.Gly1997Cys
ENST00000369850.7:c.6013G>T	ENSP00000358866.3:p.Gly2005Cys
ENST00000369856.7:c.5932G>T	ENSP00000358872.4:p.Gly1978Cys
ENST00000415241.1:c.198G>T
ENST00000420627.5:c.5969G>T	ENSP00000408921.1:n.5969G>T
ENST00000422373.5:c.5989G>T	ENSP00000416926.1:p.Gly1997Cys
ENST00000438732.2:c.687G>T
ENST00000466325.1:n.152G>T
ENST00000490936.5:n.2002G>T
ENST00000610817.4:c.5844+88G>T	ENSP00000480593.1:n.5844+88G>T
NM_001110556.1:c.6013G>T	NP_001104026.1:p.Gly2005Cys
NM_001456.3:c.5989G>T	NP_001447.2:p.Gly1997Cys
XM_011531127.1:c.5917G>T	XP_011529429.1:p.Gly1973Cys
XM_011531128.1:c.5893G>T	XP_011529430.1:p.Gly1965Cys
XM_011531129.1:c.5839G>T	XP_011529431.1:p.Gly1947Cys
XM_011531130.1:c.5815G>T	XP_011529432.1:p.Gly1939Cys
XM_011531131.1:c.5812G>T	XP_011529433.1:p.Gly1938Cys
NM_001110556.2:c.6013G>T MANE Select	NP_001104026.1:p.Gly2005Cys
NM_001456.4:c.5989G>T	NP_001447.2:p.Gly1997Cys