Canonical Allele Identifier: CA415197448

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581721G>T (hg19) ; chrX:g.154353353G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353353G>T , CM000685.2:g.154353353G>T	GRCh38
NC_000023.10:g.153581721G>T , CM000685.1:g.153581721G>T	GRCh37
NC_000023.9:g.153234915G>T	NCBI36
NG_011506.1:g.26286C>A
NG_011506.2:g.26286C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5941C>A	ENSP00000353467.4:p.Pro1981Thr
ENST00000369850.10:c.5965C>A MANE Select	ENSP00000358866.3:p.Pro1989Thr
ENST00000369856.8:c.5884C>A	ENSP00000358872.4:p.Pro1962Thr
ENST00000422373.6:c.3161-678C>A	ENSP00000416926.2:n.3161-678C>A
ENST00000610817.5:c.6022C>A	ENSP00000480593.2:n.6022C>A
ENST00000673639.2:c.280-4663C>A
ENST00000676696.1:c.6244C>A	ENSP00000503392.1:n.6244C>A
ENST00000678304.1:n.1144C>A
ENST00000344736.8:c.5845C>A	ENSP00000358863.3:p.Pro1949Thr
ENST00000360319.8:c.5941C>A	ENSP00000353467.4:p.Pro1981Thr
ENST00000369850.7:c.5965C>A	ENSP00000358866.3:p.Pro1989Thr
ENST00000369856.7:c.5884C>A	ENSP00000358872.4:p.Pro1962Thr
ENST00000415241.1:c.150C>A
ENST00000420627.5:c.5921C>A	ENSP00000408921.1:n.5921C>A
ENST00000422373.5:c.5941C>A	ENSP00000416926.1:p.Pro1981Thr
ENST00000438732.2:c.639C>A
ENST00000466325.1:n.104C>A
ENST00000490936.5:n.1954C>A
ENST00000610817.4:c.5844+40C>A	ENSP00000480593.1:n.5844+40C>A
NM_001110556.1:c.5965C>A	NP_001104026.1:p.Pro1989Thr
NM_001456.3:c.5941C>A	NP_001447.2:p.Pro1981Thr
XM_011531127.1:c.5869C>A	XP_011529429.1:p.Pro1957Thr
XM_011531128.1:c.5845C>A	XP_011529430.1:p.Pro1949Thr
XM_011531129.1:c.5791C>A	XP_011529431.1:p.Pro1931Thr
XM_011531130.1:c.5767C>A	XP_011529432.1:p.Pro1923Thr
XM_011531131.1:c.5764C>A	XP_011529433.1:p.Pro1922Thr
NM_001110556.2:c.5965C>A MANE Select	NP_001104026.1:p.Pro1989Thr
NM_001456.4:c.5941C>A	NP_001447.2:p.Pro1981Thr