Canonical Allele Identifier: CA2739249492
Gene: FLNA HGNC NCBI

Linked Data

dbSNP Id: rs2148122552

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371472dup , CM000685.2:g.154371472dup GRCh38
NC_000023.10:g.153599840dup , CM000685.1:g.153599840dup GRCh37
NC_000023.9:g.153253034dup NCBI36
NG_008677.1:g.2045dup , LRG_745:g.2045dup
NG_011506.1:g.8170dup
NG_011506.2:g.8170dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369850.10:c.-116-108dup MANE Select ENSP00000358866.3:n.-116-108dup
ENST00000369850.7:c.-116-108dup ENSP00000358866.3:n.-116-108dup
ENST00000422373.5:c.-116-108dup ENSP00000416926.1:n.-116-108dup
ENST00000610817.4:c.-197-108dup ENSP00000480593.1:n.-197-108dup
NM_001110556.1:c.-116-108dup NP_001104026.1:n.-116-108dup
NM_001456.3:c.-116-108dup NP_001447.2:n.-116-108dup
XM_011531127.1:c.-116-108dup XP_011529429.1:n.-116-108dup
XM_011531128.1:c.-116-108dup XP_011529430.1:n.-116-108dup
XM_011531129.1:c.-116-108dup XP_011529431.1:n.-116-108dup
XM_011531130.1:c.-116-108dup XP_011529432.1:n.-116-108dup
XM_011531131.1:c.-116-108dup XP_011529433.1:n.-116-108dup
NM_001110556.2:c.-116-108dup MANE Select NP_001104026.1:n.-116-108dup
NM_001456.4:c.-116-108dup NP_001447.2:n.-116-108dup