Canonical Allele Identifier: CA2695114235
Gene: FLNA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371424_154371432del , CM000685.2:g.154371424_154371432del GRCh38
NC_000023.10:g.153599792_153599800del , CM000685.1:g.153599792_153599800del GRCh37
NC_000023.9:g.153252986_153252994del NCBI36
NG_008677.1:g.1997_2005del , LRG_745:g.1997_2005del
NG_011506.1:g.8208_8216del
NG_011506.2:g.8208_8216del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369850.10:c.-116-70_-116-62del MANE Select ENSP00000358866.3:n.-116-70_-116-62del
ENST00000369850.7:c.-116-70_-116-62del ENSP00000358866.3:n.-116-70_-116-62del
ENST00000422373.5:c.-116-70_-116-62del ENSP00000416926.1:n.-116-70_-116-62del
ENST00000610817.4:c.-197-70_-197-62del ENSP00000480593.1:n.-197-70_-197-62del
NM_001110556.1:c.-116-70_-116-62del NP_001104026.1:n.-116-70_-116-62del
NM_001456.3:c.-116-70_-116-62del NP_001447.2:n.-116-70_-116-62del
XM_011531127.1:c.-116-70_-116-62del XP_011529429.1:n.-116-70_-116-62del
XM_011531128.1:c.-116-70_-116-62del XP_011529430.1:n.-116-70_-116-62del
XM_011531129.1:c.-116-70_-116-62del XP_011529431.1:n.-116-70_-116-62del
XM_011531130.1:c.-116-70_-116-62del XP_011529432.1:n.-116-70_-116-62del
XM_011531131.1:c.-116-70_-116-62del XP_011529433.1:n.-116-70_-116-62del
NM_001110556.2:c.-116-70_-116-62del MANE Select NP_001104026.1:n.-116-70_-116-62del
NM_001456.4:c.-116-70_-116-62del NP_001447.2:n.-116-70_-116-62del