Canonical Allele Identifier: CA16043288
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 373811
ClinVar RCV Id: RCV000414405
dbSNP Id: rs1057518626

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154361788del , CM000685.2:g.154361788del GRCh38
NC_000023.10:g.153590156del , CM000685.1:g.153590156del GRCh37
NC_000023.9:g.153243350del NCBI36
NG_011506.1:g.17853del
NG_011506.2:g.17853del

Transcript Alleles

HGVS Amino-acid change
ENST00000360319.9:c.2828del
ENST00000369850.10:c.2828del
ENST00000369856.8:c.2747del
ENST00000422373.6:c.2828del
ENST00000610817.5:c.2885del
ENST00000673639.2:c.279+3650del
ENST00000676696.1:c.3107del
ENST00000344736.8:c.2828del
ENST00000360319.8:c.2828del
ENST00000369850.7:c.2828del
ENST00000369856.7:c.2747del
ENST00000420627.5:c.2784del
ENST00000422373.5:c.2828del
ENST00000610817.4:c.2747del
NM_001110556.1:c.2828del
NM_001456.3:c.2828del
XM_011531127.1:c.2828del
XM_011531128.1:c.2828del
XM_011531129.1:c.2828del
XM_011531130.1:c.2828del
XM_011531131.1:c.2627del
NM_001110556.2:c.2828del
NM_001456.4:c.2828del