Canonical Allele Identifier: CA519709779

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153596106_153596208del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154367740_154367842del , CM000685.2:g.154367740_154367842del	GRCh38
NC_000023.10:g.153596108_153596210del , CM000685.1:g.153596108_153596210del	GRCh37
NC_000023.9:g.153249302_153249404del	NCBI36
NG_011506.1:g.11799_11901del
NG_011506.2:g.11799_11901del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.622+2_623del
ENST00000369850.10:c.622+2_623del
ENST00000369856.8:c.541+2_542del
ENST00000422373.6:c.622+2_623del
ENST00000610817.5:c.622+2_623del
ENST00000676696.1:c.622+2_623del
ENST00000344736.8:c.622+2_623del
ENST00000360319.8:c.622+2_623del
ENST00000369850.7:c.622+2_623del
ENST00000369856.7:c.541+2_542del
ENST00000420627.5:c.580+2_581del
ENST00000422373.5:c.622+2_623del
ENST00000610817.4:c.541+2_542del
NM_001110556.1:c.622+2_623del
NM_001456.3:c.622+2_623del
XM_011531127.1:c.622+2_623del
XM_011531128.1:c.622+2_623del
XM_011531129.1:c.622+2_623del
XM_011531130.1:c.622+2_623del
XM_011531131.1:c.622+2_623del
NM_001110556.2:c.622+2_623del
NM_001456.4:c.622+2_623del