Canonical Allele Identifier: CA147282

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352308C>G , CM000685.2:g.154352308C>G	GRCh38
NC_000023.10:g.153580676C>G , CM000685.1:g.153580676C>G	GRCh37
NC_000023.9:g.153233870C>G	NCBI36
NG_011506.1:g.27331G>C
NG_011506.2:g.27331G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6618G>C	ENSP00000353467.4:p.Val2206=
ENST00000369850.10:c.6642G>C MANE Select	ENSP00000358866.3:p.Val2214=
ENST00000369856.8:c.6561G>C	ENSP00000358872.4:p.Val2187=
ENST00000422373.6:c.3423G>C	ENSP00000416926.2:p.Val1141=
ENST00000610817.5:c.6699G>C	ENSP00000480593.2:n.6699G>C
ENST00000673639.2:c.280-3618G>C
ENST00000676696.1:c.6921G>C	ENSP00000503392.1:n.6921G>C
ENST00000678304.1:n.1821G>C
ENST00000344736.8:c.6522G>C	ENSP00000358863.3:p.Val2174=
ENST00000360319.8:c.6618G>C	ENSP00000353467.4:p.Val2206=
ENST00000369850.7:c.6642G>C	ENSP00000358866.3:p.Val2214=
ENST00000369856.7:c.6561G>C	ENSP00000358872.4:p.Val2187=
ENST00000420627.5:c.6598G>C	ENSP00000408921.1:n.6598G>C
ENST00000422373.5:c.6618G>C	ENSP00000416926.1:p.Val2206=
ENST00000444578.1:c.462G>C	ENSP00000397824.1:p.Val154=
ENST00000474358.5:n.275G>C
ENST00000490936.5:n.2631G>C
ENST00000498411.1:n.67+509G>C
ENST00000610817.4:c.5845-358G>C	ENSP00000480593.1:n.5845-358G>C
NM_001110556.1:c.6642G>C	NP_001104026.1:p.Val2214=
NM_001456.3:c.6618G>C	NP_001447.2:p.Val2206=
XM_011531127.1:c.6546G>C	XP_011529429.1:p.Val2182=
XM_011531128.1:c.6522G>C	XP_011529430.1:p.Val2174=
XM_011531129.1:c.6468G>C	XP_011529431.1:p.Val2156=
XM_011531130.1:c.6444G>C	XP_011529432.1:p.Val2148=
XM_011531131.1:c.6441G>C	XP_011529433.1:p.Val2147=
NM_001110556.2:c.6642G>C MANE Select	NP_001104026.1:p.Val2214=
NM_001456.4:c.6618G>C	NP_001447.2:p.Val2206=