Canonical Allele Identifier: CA645171446

Gene: FLNA

Linked Data

• dbSNP Id: rs1332823416
• gnomAD v2: X-153599015-CCGGGGCGCAGCGGG-C
• gnomAD v3: X-154370647-CCGGGGCGCAGCGGG-C
• gnomAD v4: X-154370647-CCGGGGCGCAGCGGG-C
• MyVariant Identifiers: chrX:g.153599016_153599029del (hg19) ; chrX:g.154370648_154370661del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154370653_154370666del , CM000685.2:g.154370653_154370666del	GRCh38
NC_000023.10:g.153599021_153599034del , CM000685.1:g.153599021_153599034del	GRCh37
NC_000023.9:g.153252215_153252228del	NCBI36
NG_008677.1:g.1226_1239del , LRG_745:g.1226_1239del
NG_011506.1:g.8978_8991del
NG_011506.2:g.8978_8991del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.373+212_373+225del	ENSP00000353467.4:n.373+212_373+225del
ENST00000369850.10:c.373+212_373+225del MANE Select	ENSP00000358866.3:n.373+212_373+225del
ENST00000369856.8:c.292+212_292+225del	ENSP00000358872.4:n.292+212_292+225del
ENST00000422373.6:c.373+212_373+225del	ENSP00000416926.2:n.373+212_373+225del
ENST00000610817.5:c.373+212_373+225del	ENSP00000480593.2:n.373+212_373+225del
ENST00000676696.1:c.373+212_373+225del	ENSP00000503392.1:n.373+212_373+225del
ENST00000344736.8:c.373+212_373+225del	ENSP00000358863.3:n.373+212_373+225del
ENST00000360319.8:c.373+212_373+225del	ENSP00000353467.4:n.373+212_373+225del
ENST00000369850.7:c.373+212_373+225del	ENSP00000358866.3:n.373+212_373+225del
ENST00000369856.7:c.292+212_292+225del	ENSP00000358872.4:n.292+212_292+225del
ENST00000420627.5:c.331+212_331+225del	ENSP00000408921.1:n.331+212_331+225del
ENST00000422373.5:c.373+212_373+225del	ENSP00000416926.1:n.373+212_373+225del
ENST00000610817.4:c.292+212_292+225del	ENSP00000480593.1:n.292+212_292+225del
NM_001110556.1:c.373+212_373+225del	NP_001104026.1:n.373+212_373+225del
NM_001456.3:c.373+212_373+225del	NP_001447.2:n.373+212_373+225del
XM_011531127.1:c.373+212_373+225del	XP_011529429.1:n.373+212_373+225del
XM_011531128.1:c.373+212_373+225del	XP_011529430.1:n.373+212_373+225del
XM_011531129.1:c.373+212_373+225del	XP_011529431.1:n.373+212_373+225del
XM_011531130.1:c.373+212_373+225del	XP_011529432.1:n.373+212_373+225del
XM_011531131.1:c.373+212_373+225del	XP_011529433.1:n.373+212_373+225del
NM_001110556.2:c.373+212_373+225del MANE Select	NP_001104026.1:n.373+212_373+225del
NM_001456.4:c.373+212_373+225del	NP_001447.2:n.373+212_373+225del