Canonical Allele Identifier: CA10560442
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 464998
dbSNP Id: rs372673802

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154357431C>T , CM000685.2:g.154357431C>T GRCh38
NC_000023.10:g.153585799C>T , CM000685.1:g.153585799C>T GRCh37
NC_000023.9:g.153238993C>T NCBI36
NG_011506.1:g.22208G>A
NG_011506.2:g.22208G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.4945+3G>A ENSP00000353467.4:n.4945+3G>A
ENST00000369850.10:c.4945+3G>A MANE Select ENSP00000358866.3:n.4945+3G>A
ENST00000369856.8:c.4864+3G>A ENSP00000358872.4:n.4864+3G>A
ENST00000422373.6:c.3160+3924G>A ENSP00000416926.2:n.3160+3924G>A
ENST00000610817.5:c.5002+3G>A ENSP00000480593.2:n.5002+3G>A
ENST00000673639.2:c.279+8005G>A
ENST00000676696.1:c.5224+3G>A ENSP00000503392.1:n.5224+3G>A
ENST00000678304.1:n.148+1658G>A
ENST00000344736.8:c.4945+3G>A ENSP00000358863.3:n.4945+3G>A
ENST00000360319.8:c.4945+3G>A ENSP00000353467.4:n.4945+3G>A
ENST00000369850.7:c.4945+3G>A ENSP00000358866.3:n.4945+3G>A
ENST00000369856.7:c.4864+3G>A ENSP00000358872.4:n.4864+3G>A
ENST00000420627.5:c.4901+3G>A ENSP00000408921.1:n.4901+3G>A
ENST00000422373.5:c.4945+3G>A ENSP00000416926.1:n.4945+3G>A
ENST00000490936.5:n.958+3G>A
ENST00000610817.4:c.4864+3G>A ENSP00000480593.1:n.4864+3G>A
NM_001110556.1:c.4945+3G>A NP_001104026.1:n.4945+3G>A
NM_001456.3:c.4945+3G>A NP_001447.2:n.4945+3G>A
XM_011531127.1:c.4945+3G>A XP_011529429.1:n.4945+3G>A
XM_011531128.1:c.4945+3G>A XP_011529430.1:n.4945+3G>A
XM_011531129.1:c.4945+3G>A XP_011529431.1:n.4945+3G>A
XM_011531130.1:c.4945+3G>A XP_011529432.1:n.4945+3G>A
XM_011531131.1:c.4744+3G>A XP_011529433.1:n.4744+3G>A
NM_001110556.2:c.4945+3G>A MANE Select NP_001104026.1:n.4945+3G>A
NM_001456.4:c.4945+3G>A NP_001447.2:n.4945+3G>A