Canonical Allele Identifier: CA2466660597
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371442_154371443delinsTG , CM000685.2:g.154371442_154371443delinsTG GRCh38
NC_000023.10:g.153599810_153599811delinsTG , CM000685.1:g.153599810_153599811delinsTG GRCh37
NC_000023.9:g.153253004_153253005delinsTG NCBI36
NG_008677.1:g.2015_2016delinsTG , LRG_745:g.2015_2016delinsTG
NG_011506.1:g.8196_8197delinsCA
NG_011506.2:g.8196_8197delinsCA

Transcript Alleles

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