Canonical Allele Identifier: CA415194696

Gene: FLNA

Linked Data

• COSMIC: COSM4972936 ; COSM4972937
• MyVariant Identifiers: chrX:g.153581289T>G (hg19) ; chrX:g.154352921T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352921T>G , CM000685.2:g.154352921T>G	GRCh38
NC_000023.10:g.153581289T>G , CM000685.1:g.153581289T>G	GRCh37
NC_000023.9:g.153234483T>G	NCBI36
NG_011506.1:g.26718A>C
NG_011506.2:g.26718A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6206A>C	ENSP00000353467.4:p.Tyr2069Ser
ENST00000369850.10:c.6230A>C MANE Select	ENSP00000358866.3:p.Tyr2077Ser
ENST00000369856.8:c.6149A>C	ENSP00000358872.4:p.Tyr2050Ser
ENST00000422373.6:c.3161-246A>C	ENSP00000416926.2:n.3161-246A>C
ENST00000610817.5:c.6287A>C	ENSP00000480593.2:n.6287A>C
ENST00000673639.2:c.280-4231A>C
ENST00000676696.1:c.6509A>C	ENSP00000503392.1:n.6509A>C
ENST00000678304.1:n.1409A>C
ENST00000344736.8:c.6110A>C	ENSP00000358863.3:p.Tyr2037Ser
ENST00000360319.8:c.6206A>C	ENSP00000353467.4:p.Tyr2069Ser
ENST00000369850.7:c.6230A>C	ENSP00000358866.3:p.Tyr2077Ser
ENST00000369856.7:c.6149A>C	ENSP00000358872.4:p.Tyr2050Ser
ENST00000415241.1:c.432A>C
ENST00000420627.5:c.6186A>C	ENSP00000408921.1:n.6186A>C
ENST00000422373.5:c.6206A>C	ENSP00000416926.1:p.Tyr2069Ser
ENST00000444578.1:c.173A>C	ENSP00000397824.1:p.Tyr58Ser
ENST00000466325.1:n.445A>C
ENST00000490936.5:n.2219A>C
ENST00000610817.4:c.5844+472A>C	ENSP00000480593.1:n.5844+472A>C
NM_001110556.1:c.6230A>C	NP_001104026.1:p.Tyr2077Ser
NM_001456.3:c.6206A>C	NP_001447.2:p.Tyr2069Ser
XM_011531127.1:c.6134A>C	XP_011529429.1:p.Tyr2045Ser
XM_011531128.1:c.6110A>C	XP_011529430.1:p.Tyr2037Ser
XM_011531129.1:c.6056A>C	XP_011529431.1:p.Tyr2019Ser
XM_011531130.1:c.6032A>C	XP_011529432.1:p.Tyr2011Ser
XM_011531131.1:c.6029A>C	XP_011529433.1:p.Tyr2010Ser
NM_001110556.2:c.6230A>C MANE Select	NP_001104026.1:p.Tyr2077Ser
NM_001456.4:c.6206A>C	NP_001447.2:p.Tyr2069Ser