Canonical Allele Identifier: CA415235462
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1516255
ClinVar RCV Id: RCV002023815
dbSNP Id: rs1488268931

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154362328G>A , CM000685.2:g.154362328G>A GRCh38
NC_000023.10:g.153590696G>A , CM000685.1:g.153590696G>A GRCh37
NC_000023.9:g.153243890G>A NCBI36
NG_011506.1:g.17311C>T
NG_011506.2:g.17311C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.2570C>T ENSP00000353467.4:p.Thr857Met
ENST00000369850.10:c.2570C>T MANE Select ENSP00000358866.3:p.Thr857Met
ENST00000369856.8:c.2489C>T ENSP00000358872.4:p.Thr830Met
ENST00000422373.6:c.2570C>T ENSP00000416926.2:p.Thr857Met
ENST00000610817.5:c.2627C>T ENSP00000480593.2:n.2627C>T
ENST00000673639.2:c.279+3108C>T
ENST00000676696.1:c.2849C>T ENSP00000503392.1:n.2849C>T
ENST00000344736.8:c.2570C>T ENSP00000358863.3:p.Thr857Met
ENST00000360319.8:c.2570C>T ENSP00000353467.4:p.Thr857Met
ENST00000369850.7:c.2570C>T ENSP00000358866.3:p.Thr857Met
ENST00000369856.7:c.2489C>T ENSP00000358872.4:p.Thr830Met
ENST00000420627.5:c.2526C>T ENSP00000408921.1:n.2526C>T
ENST00000422373.5:c.2570C>T ENSP00000416926.1:p.Thr857Met
ENST00000610817.4:c.2489C>T ENSP00000480593.1:p.Thr830Met
NM_001110556.1:c.2570C>T NP_001104026.1:p.Thr857Met
NM_001456.3:c.2570C>T NP_001447.2:p.Thr857Met
XM_011531127.1:c.2570C>T XP_011529429.1:p.Thr857Met
XM_011531128.1:c.2570C>T XP_011529430.1:p.Thr857Met
XM_011531129.1:c.2570C>T XP_011529431.1:p.Thr857Met
XM_011531130.1:c.2570C>T XP_011529432.1:p.Thr857Met
XM_011531131.1:c.2369C>T XP_011529433.1:p.Thr790Met
NM_001110556.2:c.2570C>T MANE Select NP_001104026.1:p.Thr857Met
NM_001456.4:c.2570C>T NP_001447.2:p.Thr857Met