Canonical Allele Identifier: CA873314826

Gene: FLNA

Linked Data

• dbSNP Id: rs1402435843
• gnomAD v3: X-154371394-GGAGGGCGGGGCCA-G
• gnomAD v4: X-154371394-GGAGGGCGGGGCCA-G
• MyVariant Identifiers: chrX:g.154371395_154371407del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371404_154371416del , CM000685.2:g.154371404_154371416del	GRCh38
NC_000023.10:g.153599772_153599784del , CM000685.1:g.153599772_153599784del	GRCh37
NC_000023.9:g.153252966_153252978del	NCBI36
NG_008677.1:g.1977_1989del , LRG_745:g.1977_1989del
NG_011506.1:g.8232_8244del
NG_011506.2:g.8232_8244del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-116-46_-116-34del MANE Select	ENSP00000358866.3:n.-116-46_-116-34del
ENST00000369850.7:c.-116-46_-116-34del	ENSP00000358866.3:n.-116-46_-116-34del
ENST00000422373.5:c.-116-46_-116-34del	ENSP00000416926.1:n.-116-46_-116-34del
ENST00000610817.4:c.-197-46_-197-34del	ENSP00000480593.1:n.-197-46_-197-34del
NM_001110556.1:c.-116-46_-116-34del	NP_001104026.1:n.-116-46_-116-34del
NM_001456.3:c.-116-46_-116-34del	NP_001447.2:n.-116-46_-116-34del
XM_011531127.1:c.-116-46_-116-34del	XP_011529429.1:n.-116-46_-116-34del
XM_011531128.1:c.-116-46_-116-34del	XP_011529430.1:n.-116-46_-116-34del
XM_011531129.1:c.-116-46_-116-34del	XP_011529431.1:n.-116-46_-116-34del
XM_011531130.1:c.-116-46_-116-34del	XP_011529432.1:n.-116-46_-116-34del
XM_011531131.1:c.-116-46_-116-34del	XP_011529433.1:n.-116-46_-116-34del
NM_001110556.2:c.-116-46_-116-34del MANE Select	NP_001104026.1:n.-116-46_-116-34del
NM_001456.4:c.-116-46_-116-34del	NP_001447.2:n.-116-46_-116-34del