Canonical Allele Identifier: CA10561473
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435210
dbSNP Id: rs782292045

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371221C>A , CM000685.2:g.154371221C>A GRCh38
NC_000023.10:g.153599589C>A , CM000685.1:g.153599589C>A GRCh37
NC_000023.9:g.153252783C>A NCBI36
NG_008677.1:g.1794C>A , LRG_745:g.1794C>A
NG_011506.1:g.8418G>T
NG_011506.2:g.8418G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.25G>T ENSP00000353467.4:p.Gly9Cys
ENST00000369850.10:c.25G>T MANE Select ENSP00000358866.3:p.Gly9Cys
ENST00000369856.8:c.-57G>T ENSP00000358872.4:n.-57G>T
ENST00000422373.6:c.25G>T ENSP00000416926.2:p.Gly9Cys
ENST00000610817.5:c.25G>T ENSP00000480593.2:p.Gly9Cys
ENST00000676696.1:c.25G>T ENSP00000503392.1:p.Gly9Cys
ENST00000344736.8:c.25G>T ENSP00000358863.3:p.Gly9Cys
ENST00000360319.8:c.25G>T ENSP00000353467.4:p.Gly9Cys
ENST00000369850.7:c.25G>T ENSP00000358866.3:p.Gly9Cys
ENST00000369856.7:c.-57G>T ENSP00000358872.4:n.-57G>T
ENST00000422373.5:c.25G>T ENSP00000416926.1:p.Gly9Cys
ENST00000610817.4:c.-57G>T ENSP00000480593.1:n.-57G>T
NM_001110556.1:c.25G>T NP_001104026.1:p.Gly9Cys
NM_001456.3:c.25G>T NP_001447.2:p.Gly9Cys
XM_011531127.1:c.25G>T XP_011529429.1:p.Gly9Cys
XM_011531128.1:c.25G>T XP_011529430.1:p.Gly9Cys
XM_011531129.1:c.25G>T XP_011529431.1:p.Gly9Cys
XM_011531130.1:c.25G>T XP_011529432.1:p.Gly9Cys
XM_011531131.1:c.25G>T XP_011529433.1:p.Gly9Cys
NM_001110556.2:c.25G>T MANE Select NP_001104026.1:p.Gly9Cys
NM_001456.4:c.25G>T NP_001447.2:p.Gly9Cys