Canonical Allele Identifier: CA415196128

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581495G>T (hg19) ; chrX:g.154353127G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353127G>T , CM000685.2:g.154353127G>T	GRCh38
NC_000023.10:g.153581495G>T , CM000685.1:g.153581495G>T	GRCh37
NC_000023.9:g.153234689G>T	NCBI36
NG_011506.1:g.26512C>A
NG_011506.2:g.26512C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6076C>A	ENSP00000353467.4:p.Pro2026Thr
ENST00000369850.10:c.6100C>A MANE Select	ENSP00000358866.3:p.Pro2034Thr
ENST00000369856.8:c.6019C>A	ENSP00000358872.4:p.Pro2007Thr
ENST00000422373.6:c.3161-452C>A	ENSP00000416926.2:n.3161-452C>A
ENST00000610817.5:c.6157C>A	ENSP00000480593.2:n.6157C>A
ENST00000673639.2:c.280-4437C>A
ENST00000676696.1:c.6379C>A	ENSP00000503392.1:n.6379C>A
ENST00000678304.1:n.1279C>A
ENST00000344736.8:c.5980C>A	ENSP00000358863.3:p.Pro1994Thr
ENST00000360319.8:c.6076C>A	ENSP00000353467.4:p.Pro2026Thr
ENST00000369850.7:c.6100C>A	ENSP00000358866.3:p.Pro2034Thr
ENST00000369856.7:c.6019C>A	ENSP00000358872.4:p.Pro2007Thr
ENST00000415241.1:c.302C>A
ENST00000420627.5:c.6056C>A	ENSP00000408921.1:n.6056C>A
ENST00000422373.5:c.6076C>A	ENSP00000416926.1:p.Pro2026Thr
ENST00000444578.1:c.43C>A	ENSP00000397824.1:p.Pro15Thr
ENST00000466325.1:n.239C>A
ENST00000490936.5:n.2089C>A
ENST00000610817.4:c.5844+266C>A	ENSP00000480593.1:n.5844+266C>A
NM_001110556.1:c.6100C>A	NP_001104026.1:p.Pro2034Thr
NM_001456.3:c.6076C>A	NP_001447.2:p.Pro2026Thr
XM_011531127.1:c.6004C>A	XP_011529429.1:p.Pro2002Thr
XM_011531128.1:c.5980C>A	XP_011529430.1:p.Pro1994Thr
XM_011531129.1:c.5926C>A	XP_011529431.1:p.Pro1976Thr
XM_011531130.1:c.5902C>A	XP_011529432.1:p.Pro1968Thr
XM_011531131.1:c.5899C>A	XP_011529433.1:p.Pro1967Thr
NM_001110556.2:c.6100C>A MANE Select	NP_001104026.1:p.Pro2034Thr
NM_001456.4:c.6076C>A	NP_001447.2:p.Pro2026Thr