Canonical Allele Identifier: CA415195827

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581458T>C (hg19) ; chrX:g.154353090T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353090T>C , CM000685.2:g.154353090T>C	GRCh38
NC_000023.10:g.153581458T>C , CM000685.1:g.153581458T>C	GRCh37
NC_000023.9:g.153234652T>C	NCBI36
NG_011506.1:g.26549A>G
NG_011506.2:g.26549A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6113A>G	ENSP00000353467.4:p.Asp2038Gly
ENST00000369850.10:c.6137A>G MANE Select	ENSP00000358866.3:p.Asp2046Gly
ENST00000369856.8:c.6056A>G	ENSP00000358872.4:p.Asp2019Gly
ENST00000422373.6:c.3161-415A>G	ENSP00000416926.2:n.3161-415A>G
ENST00000610817.5:c.6194A>G	ENSP00000480593.2:n.6194A>G
ENST00000673639.2:c.280-4400A>G
ENST00000676696.1:c.6416A>G	ENSP00000503392.1:n.6416A>G
ENST00000678304.1:n.1316A>G
ENST00000344736.8:c.6017A>G	ENSP00000358863.3:p.Asp2006Gly
ENST00000360319.8:c.6113A>G	ENSP00000353467.4:p.Asp2038Gly
ENST00000369850.7:c.6137A>G	ENSP00000358866.3:p.Asp2046Gly
ENST00000369856.7:c.6056A>G	ENSP00000358872.4:p.Asp2019Gly
ENST00000415241.1:c.339A>G
ENST00000420627.5:c.6093A>G	ENSP00000408921.1:n.6093A>G
ENST00000422373.5:c.6113A>G	ENSP00000416926.1:p.Asp2038Gly
ENST00000444578.1:c.80A>G	ENSP00000397824.1:p.Asp27Gly
ENST00000466325.1:n.276A>G
ENST00000490936.5:n.2126A>G
ENST00000610817.4:c.5844+303A>G	ENSP00000480593.1:n.5844+303A>G
NM_001110556.1:c.6137A>G	NP_001104026.1:p.Asp2046Gly
NM_001456.3:c.6113A>G	NP_001447.2:p.Asp2038Gly
XM_011531127.1:c.6041A>G	XP_011529429.1:p.Asp2014Gly
XM_011531128.1:c.6017A>G	XP_011529430.1:p.Asp2006Gly
XM_011531129.1:c.5963A>G	XP_011529431.1:p.Asp1988Gly
XM_011531130.1:c.5939A>G	XP_011529432.1:p.Asp1980Gly
XM_011531131.1:c.5936A>G	XP_011529433.1:p.Asp1979Gly
NM_001110556.2:c.6137A>G MANE Select	NP_001104026.1:p.Asp2046Gly
NM_001456.4:c.6113A>G	NP_001447.2:p.Asp2038Gly