Canonical Allele Identifier: CA415192773

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581044C>G (hg19) ; chrX:g.154352676C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352676C>G , CM000685.2:g.154352676C>G	GRCh38
NC_000023.10:g.153581044C>G , CM000685.1:g.153581044C>G	GRCh37
NC_000023.9:g.153234238C>G	NCBI36
NG_011506.1:g.26963G>C
NG_011506.2:g.26963G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6356-1G>C	ENSP00000353467.4:n.6356-1G>C
ENST00000369850.10:c.6380-1G>C MANE Select	ENSP00000358866.3:n.6380-1G>C
ENST00000369856.8:c.6299-1G>C	ENSP00000358872.4:n.6299-1G>C
ENST00000422373.6:c.3161-1G>C	ENSP00000416926.2:n.3161-1G>C
ENST00000610817.5:c.6437-1G>C	ENSP00000480593.2:n.6437-1G>C
ENST00000673639.2:c.280-3986G>C
ENST00000676696.1:c.6659-1G>C	ENSP00000503392.1:n.6659-1G>C
ENST00000678304.1:n.1559-1G>C
ENST00000344736.8:c.6260-1G>C	ENSP00000358863.3:n.6260-1G>C
ENST00000360319.8:c.6356-1G>C	ENSP00000353467.4:n.6356-1G>C
ENST00000369850.7:c.6380-1G>C	ENSP00000358866.3:n.6380-1G>C
ENST00000369856.7:c.6299-1G>C	ENSP00000358872.4:n.6299-1G>C
ENST00000415241.1:c.582-1G>C
ENST00000420627.5:c.6336-1G>C	ENSP00000408921.1:n.6336-1G>C
ENST00000422373.5:c.6356-1G>C	ENSP00000416926.1:n.6356-1G>C
ENST00000444578.1:c.322+96G>C	ENSP00000397824.1:n.322+96G>C
ENST00000466325.1:n.690G>C
ENST00000474358.5:n.13-1G>C
ENST00000490936.5:n.2369-1G>C
ENST00000498411.1:n.67+141G>C
ENST00000610817.4:c.5844+717G>C	ENSP00000480593.1:n.5844+717G>C
NM_001110556.1:c.6380-1G>C	NP_001104026.1:n.6380-1G>C
NM_001456.3:c.6356-1G>C	NP_001447.2:n.6356-1G>C
XM_011531127.1:c.6284-1G>C	XP_011529429.1:n.6284-1G>C
XM_011531128.1:c.6260-1G>C	XP_011529430.1:n.6260-1G>C
XM_011531129.1:c.6206-1G>C	XP_011529431.1:n.6206-1G>C
XM_011531130.1:c.6182-1G>C	XP_011529432.1:n.6182-1G>C
XM_011531131.1:c.6179-1G>C	XP_011529433.1:n.6179-1G>C
NM_001110556.2:c.6380-1G>C MANE Select	NP_001104026.1:n.6380-1G>C
NM_001456.4:c.6356-1G>C	NP_001447.2:n.6356-1G>C