Canonical Allele Identifier: CA415193362

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581177G>C (hg19) ; chrX:g.154352809G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352809G>C , CM000685.2:g.154352809G>C	GRCh38
NC_000023.10:g.153581177G>C , CM000685.1:g.153581177G>C	GRCh37
NC_000023.9:g.153234371G>C	NCBI36
NG_011506.1:g.26830C>G
NG_011506.2:g.26830C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6318C>G	ENSP00000353467.4:p.Tyr2106Ter
ENST00000369850.10:c.6342C>G MANE Select	ENSP00000358866.3:p.Tyr2114Ter
ENST00000369856.8:c.6261C>G	ENSP00000358872.4:p.Tyr2087Ter
ENST00000422373.6:c.3161-134C>G	ENSP00000416926.2:n.3161-134C>G
ENST00000610817.5:c.6399C>G	ENSP00000480593.2:n.6399C>G
ENST00000673639.2:c.280-4119C>G
ENST00000676696.1:c.6621C>G	ENSP00000503392.1:n.6621C>G
ENST00000678304.1:n.1521C>G
ENST00000344736.8:c.6222C>G	ENSP00000358863.3:p.Tyr2074Ter
ENST00000360319.8:c.6318C>G	ENSP00000353467.4:p.Tyr2106Ter
ENST00000369850.7:c.6342C>G	ENSP00000358866.3:p.Tyr2114Ter
ENST00000369856.7:c.6261C>G	ENSP00000358872.4:p.Tyr2087Ter
ENST00000415241.1:c.544C>G
ENST00000420627.5:c.6298C>G	ENSP00000408921.1:n.6298C>G
ENST00000422373.5:c.6318C>G	ENSP00000416926.1:p.Tyr2106Ter
ENST00000444578.1:c.285C>G	ENSP00000397824.1:p.Tyr95Ter
ENST00000466325.1:n.557C>G
ENST00000490936.5:n.2331C>G
ENST00000498411.1:n.67+8C>G
ENST00000610817.4:c.5844+584C>G	ENSP00000480593.1:n.5844+584C>G
NM_001110556.1:c.6342C>G	NP_001104026.1:p.Tyr2114Ter
NM_001456.3:c.6318C>G	NP_001447.2:p.Tyr2106Ter
XM_011531127.1:c.6246C>G	XP_011529429.1:p.Tyr2082Ter
XM_011531128.1:c.6222C>G	XP_011529430.1:p.Tyr2074Ter
XM_011531129.1:c.6168C>G	XP_011529431.1:p.Tyr2056Ter
XM_011531130.1:c.6144C>G	XP_011529432.1:p.Tyr2048Ter
XM_011531131.1:c.6141C>G	XP_011529433.1:p.Tyr2047Ter
NM_001110556.2:c.6342C>G MANE Select	NP_001104026.1:p.Tyr2114Ter
NM_001456.4:c.6318C>G	NP_001447.2:p.Tyr2106Ter