Canonical Allele Identifier: CA2824295720
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371441_154371442insGGGGGGGGGGGGGG , CM000685.2:g.154371441_154371442insGGGGGGGGGGGGGG GRCh38
NC_000023.10:g.153599809_153599810insGGGGGGGGGGGGGG , CM000685.1:g.153599809_153599810insGGGGGGGGGGGGGG GRCh37
NC_000023.9:g.153253003_153253004insGGGGGGGGGGGGGG NCBI36
NG_008677.1:g.2014_2015insGGGGGGGGGGGGGG , LRG_745:g.2014_2015insGGGGGGGGGGGGGG
NG_011506.1:g.8201_8202insCCCCCCCCCCCCCC
NG_011506.2:g.8201_8202insCCCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369850.10:c.-116-77_-116-76insCCCCCCCCCCCCCC MANE Select ENSP00000358866.3:n.-116-77_-116-76insCCCCCCCCCCCCCC
ENST00000369850.7:c.-116-77_-116-76insCCCCCCCCCCCCCC ENSP00000358866.3:n.-116-77_-116-76insCCCCCCCCCCCCCC
ENST00000422373.5:c.-116-77_-116-76insCCCCCCCCCCCCCC ENSP00000416926.1:n.-116-77_-116-76insCCCCCCCCCCCCCC
ENST00000610817.4:c.-197-77_-197-76insCCCCCCCCCCCCCC ENSP00000480593.1:n.-197-77_-197-76insCCCCCCCCCCCCCC
NM_001110556.1:c.-116-77_-116-76insCCCCCCCCCCCCCC NP_001104026.1:n.-116-77_-116-76insCCCCCCCCCCCCCC
NM_001456.3:c.-116-77_-116-76insCCCCCCCCCCCCCC NP_001447.2:n.-116-77_-116-76insCCCCCCCCCCCCCC
XM_011531127.1:c.-116-77_-116-76insCCCCCCCCCCCCCC XP_011529429.1:n.-116-77_-116-76insCCCCCCCCCCCCCC
XM_011531128.1:c.-116-77_-116-76insCCCCCCCCCCCCCC XP_011529430.1:n.-116-77_-116-76insCCCCCCCCCCCCCC
XM_011531129.1:c.-116-77_-116-76insCCCCCCCCCCCCCC XP_011529431.1:n.-116-77_-116-76insCCCCCCCCCCCCCC
XM_011531130.1:c.-116-77_-116-76insCCCCCCCCCCCCCC XP_011529432.1:n.-116-77_-116-76insCCCCCCCCCCCCCC
XM_011531131.1:c.-116-77_-116-76insCCCCCCCCCCCCCC XP_011529433.1:n.-116-77_-116-76insCCCCCCCCCCCCCC
NM_001110556.2:c.-116-77_-116-76insCCCCCCCCCCCCCC MANE Select NP_001104026.1:n.-116-77_-116-76insCCCCCCCCCCCCCC
NM_001456.4:c.-116-77_-116-76insCCCCCCCCCCCCCC NP_001447.2:n.-116-77_-116-76insCCCCCCCCCCCCCC