Canonical Allele Identifier: CA415195855

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581462C>A (hg19) ; chrX:g.154353094C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353094C>A , CM000685.2:g.154353094C>A	GRCh38
NC_000023.10:g.153581462C>A , CM000685.1:g.153581462C>A	GRCh37
NC_000023.9:g.153234656C>A	NCBI36
NG_011506.1:g.26545G>T
NG_011506.2:g.26545G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6109G>T	ENSP00000353467.4:p.Gly2037Trp
ENST00000369850.10:c.6133G>T MANE Select	ENSP00000358866.3:p.Gly2045Trp
ENST00000369856.8:c.6052G>T	ENSP00000358872.4:p.Gly2018Trp
ENST00000422373.6:c.3161-419G>T	ENSP00000416926.2:n.3161-419G>T
ENST00000610817.5:c.6190G>T	ENSP00000480593.2:n.6190G>T
ENST00000673639.2:c.280-4404G>T
ENST00000676696.1:c.6412G>T	ENSP00000503392.1:n.6412G>T
ENST00000678304.1:n.1312G>T
ENST00000344736.8:c.6013G>T	ENSP00000358863.3:p.Gly2005Trp
ENST00000360319.8:c.6109G>T	ENSP00000353467.4:p.Gly2037Trp
ENST00000369850.7:c.6133G>T	ENSP00000358866.3:p.Gly2045Trp
ENST00000369856.7:c.6052G>T	ENSP00000358872.4:p.Gly2018Trp
ENST00000415241.1:c.335G>T
ENST00000420627.5:c.6089G>T	ENSP00000408921.1:n.6089G>T
ENST00000422373.5:c.6109G>T	ENSP00000416926.1:p.Gly2037Trp
ENST00000444578.1:c.76G>T	ENSP00000397824.1:p.Gly26Trp
ENST00000466325.1:n.272G>T
ENST00000490936.5:n.2122G>T
ENST00000610817.4:c.5844+299G>T	ENSP00000480593.1:n.5844+299G>T
NM_001110556.1:c.6133G>T	NP_001104026.1:p.Gly2045Trp
NM_001456.3:c.6109G>T	NP_001447.2:p.Gly2037Trp
XM_011531127.1:c.6037G>T	XP_011529429.1:p.Gly2013Trp
XM_011531128.1:c.6013G>T	XP_011529430.1:p.Gly2005Trp
XM_011531129.1:c.5959G>T	XP_011529431.1:p.Gly1987Trp
XM_011531130.1:c.5935G>T	XP_011529432.1:p.Gly1979Trp
XM_011531131.1:c.5932G>T	XP_011529433.1:p.Gly1978Trp
NM_001110556.2:c.6133G>T MANE Select	NP_001104026.1:p.Gly2045Trp
NM_001456.4:c.6109G>T	NP_001447.2:p.Gly2037Trp