Canonical Allele Identifier: CA2579737973

Gene: FLNA

Linked Data

• gnomAD v4: X-154352680-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352680A>G , CM000685.2:g.154352680A>G	GRCh38
NC_000023.10:g.153581048A>G , CM000685.1:g.153581048A>G	GRCh37
NC_000023.9:g.153234242A>G	NCBI36
NG_011506.1:g.26959T>C
NG_011506.2:g.26959T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6356-5T>C	ENSP00000353467.4:n.6356-5T>C
ENST00000369850.10:c.6380-5T>C MANE Select	ENSP00000358866.3:n.6380-5T>C
ENST00000369856.8:c.6299-5T>C	ENSP00000358872.4:n.6299-5T>C
ENST00000422373.6:c.3161-5T>C	ENSP00000416926.2:n.3161-5T>C
ENST00000610817.5:c.6437-5T>C	ENSP00000480593.2:n.6437-5T>C
ENST00000673639.2:c.280-3990T>C
ENST00000676696.1:c.6659-5T>C	ENSP00000503392.1:n.6659-5T>C
ENST00000678304.1:n.1559-5T>C
ENST00000344736.8:c.6260-5T>C	ENSP00000358863.3:n.6260-5T>C
ENST00000360319.8:c.6356-5T>C	ENSP00000353467.4:n.6356-5T>C
ENST00000369850.7:c.6380-5T>C	ENSP00000358866.3:n.6380-5T>C
ENST00000369856.7:c.6299-5T>C	ENSP00000358872.4:n.6299-5T>C
ENST00000415241.1:c.582-5T>C
ENST00000420627.5:c.6336-5T>C	ENSP00000408921.1:n.6336-5T>C
ENST00000422373.5:c.6356-5T>C	ENSP00000416926.1:n.6356-5T>C
ENST00000444578.1:c.322+92T>C	ENSP00000397824.1:n.322+92T>C
ENST00000466325.1:n.686T>C
ENST00000474358.5:n.13-5T>C
ENST00000490936.5:n.2369-5T>C
ENST00000498411.1:n.67+137T>C
ENST00000610817.4:c.5844+713T>C	ENSP00000480593.1:n.5844+713T>C
NM_001110556.1:c.6380-5T>C	NP_001104026.1:n.6380-5T>C
NM_001456.3:c.6356-5T>C	NP_001447.2:n.6356-5T>C
XM_011531127.1:c.6284-5T>C	XP_011529429.1:n.6284-5T>C
XM_011531128.1:c.6260-5T>C	XP_011529430.1:n.6260-5T>C
XM_011531129.1:c.6206-5T>C	XP_011529431.1:n.6206-5T>C
XM_011531130.1:c.6182-5T>C	XP_011529432.1:n.6182-5T>C
XM_011531131.1:c.6179-5T>C	XP_011529433.1:n.6179-5T>C
NM_001110556.2:c.6380-5T>C MANE Select	NP_001104026.1:n.6380-5T>C
NM_001456.4:c.6356-5T>C	NP_001447.2:n.6356-5T>C