Canonical Allele Identifier: CA2824295721
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371447_154371448insGGTGGGGGGGGGC , CM000685.2:g.154371447_154371448insGGTGGGGGGGGGC GRCh38
NC_000023.10:g.153599815_153599816insGGTGGGGGGGGGC , CM000685.1:g.153599815_153599816insGGTGGGGGGGGGC GRCh37
NC_000023.9:g.153253009_153253010insGGTGGGGGGGGGC NCBI36
NG_008677.1:g.2020_2021insGGTGGGGGGGGGC , LRG_745:g.2020_2021insGGTGGGGGGGGGC
NG_011506.1:g.8196_8197insCCCCCACCGCCCC
NG_011506.2:g.8196_8197insCCCCCACCGCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369850.10:c.-116-82_-116-81insCCCCCACCGCCCC MANE Select ENSP00000358866.3:n.-116-82_-116-81insCCCCCACCGCCCC
ENST00000369850.7:c.-116-82_-116-81insCCCCCACCGCCCC ENSP00000358866.3:n.-116-82_-116-81insCCCCCACCGCCCC
ENST00000422373.5:c.-116-82_-116-81insCCCCCACCGCCCC ENSP00000416926.1:n.-116-82_-116-81insCCCCCACCGCCCC
ENST00000610817.4:c.-197-82_-197-81insCCCCCACCGCCCC ENSP00000480593.1:n.-197-82_-197-81insCCCCCACCGCCCC
NM_001110556.1:c.-116-82_-116-81insCCCCCACCGCCCC NP_001104026.1:n.-116-82_-116-81insCCCCCACCGCCCC
NM_001456.3:c.-116-82_-116-81insCCCCCACCGCCCC NP_001447.2:n.-116-82_-116-81insCCCCCACCGCCCC
XM_011531127.1:c.-116-82_-116-81insCCCCCACCGCCCC XP_011529429.1:n.-116-82_-116-81insCCCCCACCGCCCC
XM_011531128.1:c.-116-82_-116-81insCCCCCACCGCCCC XP_011529430.1:n.-116-82_-116-81insCCCCCACCGCCCC
XM_011531129.1:c.-116-82_-116-81insCCCCCACCGCCCC XP_011529431.1:n.-116-82_-116-81insCCCCCACCGCCCC
XM_011531130.1:c.-116-82_-116-81insCCCCCACCGCCCC XP_011529432.1:n.-116-82_-116-81insCCCCCACCGCCCC
XM_011531131.1:c.-116-82_-116-81insCCCCCACCGCCCC XP_011529433.1:n.-116-82_-116-81insCCCCCACCGCCCC
NM_001110556.2:c.-116-82_-116-81insCCCCCACCGCCCC MANE Select NP_001104026.1:n.-116-82_-116-81insCCCCCACCGCCCC
NM_001456.4:c.-116-82_-116-81insCCCCCACCGCCCC NP_001447.2:n.-116-82_-116-81insCCCCCACCGCCCC