Canonical Allele Identifier: CA873314851

Gene: FLNA

Linked Data

• dbSNP Id: rs1182204842
• gnomAD v3: X-154371442-TG-T
• gnomAD v4: X-154371442-TG-T
• MyVariant Identifiers: chrX:g.154371443del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371446del , CM000685.2:g.154371446del	GRCh38
NC_000023.10:g.153599814del , CM000685.1:g.153599814del	GRCh37
NC_000023.9:g.153253008del	NCBI36
NG_008677.1:g.2019del , LRG_745:g.2019del
NG_011506.1:g.8196del
NG_011506.2:g.8196del

Transcript Alleles

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