Canonical Allele Identifier: CA415193639

Gene: FLNA

Linked Data

• COSMIC: COSM3844060 ; COSM3844061
• MyVariant Identifiers: chrX:g.153581202T>G (hg19) ; chrX:g.154352834T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352834T>G , CM000685.2:g.154352834T>G	GRCh38
NC_000023.10:g.153581202T>G , CM000685.1:g.153581202T>G	GRCh37
NC_000023.9:g.153234396T>G	NCBI36
NG_011506.1:g.26805A>C
NG_011506.2:g.26805A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6293A>C	ENSP00000353467.4:p.Tyr2098Ser
ENST00000369850.10:c.6317A>C MANE Select	ENSP00000358866.3:p.Tyr2106Ser
ENST00000369856.8:c.6236A>C	ENSP00000358872.4:p.Tyr2079Ser
ENST00000422373.6:c.3161-159A>C	ENSP00000416926.2:n.3161-159A>C
ENST00000610817.5:c.6374A>C	ENSP00000480593.2:n.6374A>C
ENST00000673639.2:c.280-4144A>C
ENST00000676696.1:c.6596A>C	ENSP00000503392.1:n.6596A>C
ENST00000678304.1:n.1496A>C
ENST00000344736.8:c.6197A>C	ENSP00000358863.3:p.Tyr2066Ser
ENST00000360319.8:c.6293A>C	ENSP00000353467.4:p.Tyr2098Ser
ENST00000369850.7:c.6317A>C	ENSP00000358866.3:p.Tyr2106Ser
ENST00000369856.7:c.6236A>C	ENSP00000358872.4:p.Tyr2079Ser
ENST00000415241.1:c.519A>C
ENST00000420627.5:c.6273A>C	ENSP00000408921.1:n.6273A>C
ENST00000422373.5:c.6293A>C	ENSP00000416926.1:p.Tyr2098Ser
ENST00000444578.1:c.260A>C	ENSP00000397824.1:p.Tyr87Ser
ENST00000466325.1:n.532A>C
ENST00000490936.5:n.2306A>C
ENST00000498411.1:n.50A>C
ENST00000610817.4:c.5844+559A>C	ENSP00000480593.1:n.5844+559A>C
NM_001110556.1:c.6317A>C	NP_001104026.1:p.Tyr2106Ser
NM_001456.3:c.6293A>C	NP_001447.2:p.Tyr2098Ser
XM_011531127.1:c.6221A>C	XP_011529429.1:p.Tyr2074Ser
XM_011531128.1:c.6197A>C	XP_011529430.1:p.Tyr2066Ser
XM_011531129.1:c.6143A>C	XP_011529431.1:p.Tyr2048Ser
XM_011531130.1:c.6119A>C	XP_011529432.1:p.Tyr2040Ser
XM_011531131.1:c.6116A>C	XP_011529433.1:p.Tyr2039Ser
NM_001110556.2:c.6317A>C MANE Select	NP_001104026.1:p.Tyr2106Ser
NM_001456.4:c.6293A>C	NP_001447.2:p.Tyr2098Ser