Canonical Allele Identifier: CA415197512

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581727C>G (hg19) ; chrX:g.154353359C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353359C>G , CM000685.2:g.154353359C>G	GRCh38
NC_000023.10:g.153581727C>G , CM000685.1:g.153581727C>G	GRCh37
NC_000023.9:g.153234921C>G	NCBI36
NG_011506.1:g.26280G>C
NG_011506.2:g.26280G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5935G>C	ENSP00000353467.4:p.Val1979Leu
ENST00000369850.10:c.5959G>C MANE Select	ENSP00000358866.3:p.Val1987Leu
ENST00000369856.8:c.5878G>C	ENSP00000358872.4:p.Val1960Leu
ENST00000422373.6:c.3161-684G>C	ENSP00000416926.2:n.3161-684G>C
ENST00000610817.5:c.6016G>C	ENSP00000480593.2:n.6016G>C
ENST00000673639.2:c.280-4669G>C
ENST00000676696.1:c.6238G>C	ENSP00000503392.1:n.6238G>C
ENST00000678304.1:n.1138G>C
ENST00000344736.8:c.5839G>C	ENSP00000358863.3:p.Val1947Leu
ENST00000360319.8:c.5935G>C	ENSP00000353467.4:p.Val1979Leu
ENST00000369850.7:c.5959G>C	ENSP00000358866.3:p.Val1987Leu
ENST00000369856.7:c.5878G>C	ENSP00000358872.4:p.Val1960Leu
ENST00000415241.1:c.144G>C
ENST00000420627.5:c.5915G>C	ENSP00000408921.1:n.5915G>C
ENST00000422373.5:c.5935G>C	ENSP00000416926.1:p.Val1979Leu
ENST00000438732.2:c.633G>C
ENST00000466325.1:n.98G>C
ENST00000490936.5:n.1948G>C
ENST00000610817.4:c.5844+34G>C	ENSP00000480593.1:n.5844+34G>C
NM_001110556.1:c.5959G>C	NP_001104026.1:p.Val1987Leu
NM_001456.3:c.5935G>C	NP_001447.2:p.Val1979Leu
XM_011531127.1:c.5863G>C	XP_011529429.1:p.Val1955Leu
XM_011531128.1:c.5839G>C	XP_011529430.1:p.Val1947Leu
XM_011531129.1:c.5785G>C	XP_011529431.1:p.Val1929Leu
XM_011531130.1:c.5761G>C	XP_011529432.1:p.Val1921Leu
XM_011531131.1:c.5758G>C	XP_011529433.1:p.Val1920Leu
NM_001110556.2:c.5959G>C MANE Select	NP_001104026.1:p.Val1987Leu
NM_001456.4:c.5935G>C	NP_001447.2:p.Val1979Leu