Canonical Allele Identifier: CA415195925

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581471A>T (hg19) ; chrX:g.154353103A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353103A>T , CM000685.2:g.154353103A>T	GRCh38
NC_000023.10:g.153581471A>T , CM000685.1:g.153581471A>T	GRCh37
NC_000023.9:g.153234665A>T	NCBI36
NG_011506.1:g.26536T>A
NG_011506.2:g.26536T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6100T>A	ENSP00000353467.4:p.Ser2034Thr
ENST00000369850.10:c.6124T>A MANE Select	ENSP00000358866.3:p.Ser2042Thr
ENST00000369856.8:c.6043T>A	ENSP00000358872.4:p.Ser2015Thr
ENST00000422373.6:c.3161-428T>A	ENSP00000416926.2:n.3161-428T>A
ENST00000610817.5:c.6181T>A	ENSP00000480593.2:n.6181T>A
ENST00000673639.2:c.280-4413T>A
ENST00000676696.1:c.6403T>A	ENSP00000503392.1:n.6403T>A
ENST00000678304.1:n.1303T>A
ENST00000344736.8:c.6004T>A	ENSP00000358863.3:p.Ser2002Thr
ENST00000360319.8:c.6100T>A	ENSP00000353467.4:p.Ser2034Thr
ENST00000369850.7:c.6124T>A	ENSP00000358866.3:p.Ser2042Thr
ENST00000369856.7:c.6043T>A	ENSP00000358872.4:p.Ser2015Thr
ENST00000415241.1:c.326T>A
ENST00000420627.5:c.6080T>A	ENSP00000408921.1:n.6080T>A
ENST00000422373.5:c.6100T>A	ENSP00000416926.1:p.Ser2034Thr
ENST00000444578.1:c.67T>A	ENSP00000397824.1:p.Ser23Thr
ENST00000466325.1:n.263T>A
ENST00000490936.5:n.2113T>A
ENST00000610817.4:c.5844+290T>A	ENSP00000480593.1:n.5844+290T>A
NM_001110556.1:c.6124T>A	NP_001104026.1:p.Ser2042Thr
NM_001456.3:c.6100T>A	NP_001447.2:p.Ser2034Thr
XM_011531127.1:c.6028T>A	XP_011529429.1:p.Ser2010Thr
XM_011531128.1:c.6004T>A	XP_011529430.1:p.Ser2002Thr
XM_011531129.1:c.5950T>A	XP_011529431.1:p.Ser1984Thr
XM_011531130.1:c.5926T>A	XP_011529432.1:p.Ser1976Thr
XM_011531131.1:c.5923T>A	XP_011529433.1:p.Ser1975Thr
NM_001110556.2:c.6124T>A MANE Select	NP_001104026.1:p.Ser2042Thr
NM_001456.4:c.6100T>A	NP_001447.2:p.Ser2034Thr