Canonical Allele Identifier: CA415193074

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581153G>C (hg19) ; chrX:g.154352785G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352785G>C , CM000685.2:g.154352785G>C	GRCh38
NC_000023.10:g.153581153G>C , CM000685.1:g.153581153G>C	GRCh37
NC_000023.9:g.153234347G>C	NCBI36
NG_011506.1:g.26854C>G
NG_011506.2:g.26854C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6342C>G	ENSP00000353467.4:p.Asp2114Glu
ENST00000369850.10:c.6366C>G MANE Select	ENSP00000358866.3:p.Asp2122Glu
ENST00000369856.8:c.6285C>G	ENSP00000358872.4:p.Asp2095Glu
ENST00000422373.6:c.3161-110C>G	ENSP00000416926.2:n.3161-110C>G
ENST00000610817.5:c.6423C>G	ENSP00000480593.2:n.6423C>G
ENST00000673639.2:c.280-4095C>G
ENST00000676696.1:c.6645C>G	ENSP00000503392.1:n.6645C>G
ENST00000678304.1:n.1545C>G
ENST00000344736.8:c.6246C>G	ENSP00000358863.3:p.Asp2082Glu
ENST00000360319.8:c.6342C>G	ENSP00000353467.4:p.Asp2114Glu
ENST00000369850.7:c.6366C>G	ENSP00000358866.3:p.Asp2122Glu
ENST00000369856.7:c.6285C>G	ENSP00000358872.4:p.Asp2095Glu
ENST00000415241.1:c.568C>G
ENST00000420627.5:c.6322C>G	ENSP00000408921.1:n.6322C>G
ENST00000422373.5:c.6342C>G	ENSP00000416926.1:p.Asp2114Glu
ENST00000444578.1:c.309C>G	ENSP00000397824.1:p.Asp103Glu
ENST00000466325.1:n.581C>G
ENST00000490936.5:n.2355C>G
ENST00000498411.1:n.67+32C>G
ENST00000610817.4:c.5844+608C>G	ENSP00000480593.1:n.5844+608C>G
NM_001110556.1:c.6366C>G	NP_001104026.1:p.Asp2122Glu
NM_001456.3:c.6342C>G	NP_001447.2:p.Asp2114Glu
XM_011531127.1:c.6270C>G	XP_011529429.1:p.Asp2090Glu
XM_011531128.1:c.6246C>G	XP_011529430.1:p.Asp2082Glu
XM_011531129.1:c.6192C>G	XP_011529431.1:p.Asp2064Glu
XM_011531130.1:c.6168C>G	XP_011529432.1:p.Asp2056Glu
XM_011531131.1:c.6165C>G	XP_011529433.1:p.Asp2055Glu
NM_001110556.2:c.6366C>G MANE Select	NP_001104026.1:p.Asp2122Glu
NM_001456.4:c.6342C>G	NP_001447.2:p.Asp2114Glu