Canonical Allele Identifier: CA2824295724
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371447_154371450del , CM000685.2:g.154371447_154371450del GRCh38
NC_000023.10:g.153599815_153599818del , CM000685.1:g.153599815_153599818del GRCh37
NC_000023.9:g.153253009_153253012del NCBI36
NG_008677.1:g.2020_2023del , LRG_745:g.2020_2023del
NG_011506.1:g.8189_8192del
NG_011506.2:g.8189_8192del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369850.10:c.-116-89_-116-86del MANE Select ENSP00000358866.3:n.-116-89_-116-86del
ENST00000369850.7:c.-116-89_-116-86del ENSP00000358866.3:n.-116-89_-116-86del
ENST00000422373.5:c.-116-89_-116-86del ENSP00000416926.1:n.-116-89_-116-86del
ENST00000610817.4:c.-197-89_-197-86del ENSP00000480593.1:n.-197-89_-197-86del
NM_001110556.1:c.-116-89_-116-86del NP_001104026.1:n.-116-89_-116-86del
NM_001456.3:c.-116-89_-116-86del NP_001447.2:n.-116-89_-116-86del
XM_011531127.1:c.-116-89_-116-86del XP_011529429.1:n.-116-89_-116-86del
XM_011531128.1:c.-116-89_-116-86del XP_011529430.1:n.-116-89_-116-86del
XM_011531129.1:c.-116-89_-116-86del XP_011529431.1:n.-116-89_-116-86del
XM_011531130.1:c.-116-89_-116-86del XP_011529432.1:n.-116-89_-116-86del
XM_011531131.1:c.-116-89_-116-86del XP_011529433.1:n.-116-89_-116-86del
NM_001110556.2:c.-116-89_-116-86del MANE Select NP_001104026.1:n.-116-89_-116-86del
NM_001456.4:c.-116-89_-116-86del NP_001447.2:n.-116-89_-116-86del