Canonical Allele Identifier: CA121667
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11777
ClinVar RCV Id: RCV000012544
dbSNP Id: rs267606816

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154367403C>T , CM000685.2:g.154367403C>T GRCh38
NC_000023.10:g.153595771C>T , CM000685.1:g.153595771C>T GRCh37
NC_000023.9:g.153248965C>T NCBI36
NG_011506.1:g.12236G>A
NG_011506.2:g.12236G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360319.9:c.862G>A ENSP00000353467.4:p.Gly288Arg
ENST00000369850.10:c.862G>A MANE Select ENSP00000358866.3:p.Gly288Arg
ENST00000369856.8:c.781G>A ENSP00000358872.4:p.Gly261Arg
ENST00000422373.6:c.862G>A ENSP00000416926.2:p.Gly288Arg
ENST00000610817.5:c.862G>A ENSP00000480593.2:p.Gly288Arg
ENST00000676696.1:c.862G>A ENSP00000503392.1:p.Gly288Arg
ENST00000344736.8:c.862G>A ENSP00000358863.3:p.Gly288Arg
ENST00000360319.8:c.862G>A ENSP00000353467.4:p.Gly288Arg
ENST00000369850.7:c.862G>A ENSP00000358866.3:p.Gly288Arg
ENST00000369856.7:c.781G>A ENSP00000358872.4:p.Gly261Arg
ENST00000420627.5:c.820G>A ENSP00000408921.1:p.Gly274Arg
ENST00000422373.5:c.862G>A ENSP00000416926.1:p.Gly288Arg
ENST00000610817.4:c.781G>A ENSP00000480593.1:p.Gly261Arg
NM_001110556.1:c.862G>A NP_001104026.1:p.Gly288Arg
NM_001456.3:c.862G>A NP_001447.2:p.Gly288Arg
XM_011531127.1:c.862G>A XP_011529429.1:p.Gly288Arg
XM_011531128.1:c.862G>A XP_011529430.1:p.Gly288Arg
XM_011531129.1:c.862G>A XP_011529431.1:p.Gly288Arg
XM_011531130.1:c.862G>A XP_011529432.1:p.Gly288Arg
XM_011531131.1:c.862G>A XP_011529433.1:p.Gly288Arg
NM_001110556.2:c.862G>A MANE Select NP_001104026.1:p.Gly288Arg
NM_001456.4:c.862G>A NP_001447.2:p.Gly288Arg