Canonical Allele Identifier: CA415193567

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581197G>C (hg19) ; chrX:g.154352829G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352829G>C , CM000685.2:g.154352829G>C	GRCh38
NC_000023.10:g.153581197G>C , CM000685.1:g.153581197G>C	GRCh37
NC_000023.9:g.153234391G>C	NCBI36
NG_011506.1:g.26810C>G
NG_011506.2:g.26810C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6298C>G	ENSP00000353467.4:p.Pro2100Ala
ENST00000369850.10:c.6322C>G MANE Select	ENSP00000358866.3:p.Pro2108Ala
ENST00000369856.8:c.6241C>G	ENSP00000358872.4:p.Pro2081Ala
ENST00000422373.6:c.3161-154C>G	ENSP00000416926.2:n.3161-154C>G
ENST00000610817.5:c.6379C>G	ENSP00000480593.2:n.6379C>G
ENST00000673639.2:c.280-4139C>G
ENST00000676696.1:c.6601C>G	ENSP00000503392.1:n.6601C>G
ENST00000678304.1:n.1501C>G
ENST00000344736.8:c.6202C>G	ENSP00000358863.3:p.Pro2068Ala
ENST00000360319.8:c.6298C>G	ENSP00000353467.4:p.Pro2100Ala
ENST00000369850.7:c.6322C>G	ENSP00000358866.3:p.Pro2108Ala
ENST00000369856.7:c.6241C>G	ENSP00000358872.4:p.Pro2081Ala
ENST00000415241.1:c.524C>G
ENST00000420627.5:c.6278C>G	ENSP00000408921.1:n.6278C>G
ENST00000422373.5:c.6298C>G	ENSP00000416926.1:p.Pro2100Ala
ENST00000444578.1:c.265C>G	ENSP00000397824.1:p.Pro89Ala
ENST00000466325.1:n.537C>G
ENST00000490936.5:n.2311C>G
ENST00000498411.1:n.55C>G
ENST00000610817.4:c.5844+564C>G	ENSP00000480593.1:n.5844+564C>G
NM_001110556.1:c.6322C>G	NP_001104026.1:p.Pro2108Ala
NM_001456.3:c.6298C>G	NP_001447.2:p.Pro2100Ala
XM_011531127.1:c.6226C>G	XP_011529429.1:p.Pro2076Ala
XM_011531128.1:c.6202C>G	XP_011529430.1:p.Pro2068Ala
XM_011531129.1:c.6148C>G	XP_011529431.1:p.Pro2050Ala
XM_011531130.1:c.6124C>G	XP_011529432.1:p.Pro2042Ala
XM_011531131.1:c.6121C>G	XP_011529433.1:p.Pro2041Ala
NM_001110556.2:c.6322C>G MANE Select	NP_001104026.1:p.Pro2108Ala
NM_001456.4:c.6298C>G	NP_001447.2:p.Pro2100Ala