Canonical Allele Identifier: CA2695114071
Gene: FLNA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371376_154371377del , CM000685.2:g.154371376_154371377del GRCh38
NC_000023.10:g.153599744_153599745del , CM000685.1:g.153599744_153599745del GRCh37
NC_000023.9:g.153252938_153252939del NCBI36
NG_008677.1:g.1949_1950del , LRG_745:g.1949_1950del
NG_011506.1:g.8263_8264del
NG_011506.2:g.8263_8264del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369850.10:c.-116-15_-116-14del MANE Select ENSP00000358866.3:n.-116-15_-116-14del
ENST00000369850.7:c.-116-15_-116-14del ENSP00000358866.3:n.-116-15_-116-14del
ENST00000422373.5:c.-116-15_-116-14del ENSP00000416926.1:n.-116-15_-116-14del
ENST00000610817.4:c.-197-15_-197-14del ENSP00000480593.1:n.-197-15_-197-14del
NM_001110556.1:c.-116-15_-116-14del NP_001104026.1:n.-116-15_-116-14del
NM_001456.3:c.-116-15_-116-14del NP_001447.2:n.-116-15_-116-14del
XM_011531127.1:c.-116-15_-116-14del XP_011529429.1:n.-116-15_-116-14del
XM_011531128.1:c.-116-15_-116-14del XP_011529430.1:n.-116-15_-116-14del
XM_011531129.1:c.-116-15_-116-14del XP_011529431.1:n.-116-15_-116-14del
XM_011531130.1:c.-116-15_-116-14del XP_011529432.1:n.-116-15_-116-14del
XM_011531131.1:c.-116-15_-116-14del XP_011529433.1:n.-116-15_-116-14del
NM_001110556.2:c.-116-15_-116-14del MANE Select NP_001104026.1:n.-116-15_-116-14del
NM_001456.4:c.-116-15_-116-14del NP_001447.2:n.-116-15_-116-14del