Canonical Allele Identifier: CA519706144

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581292_153581367del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352927_154353002del , CM000685.2:g.154352927_154353002del	GRCh38
NC_000023.10:g.153581295_153581370del , CM000685.1:g.153581295_153581370del	GRCh37
NC_000023.9:g.153234489_153234564del	NCBI36
NG_011506.1:g.26640_26715del
NG_011506.2:g.26640_26715del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6202+2_6203del
ENST00000369850.10:c.6226+2_6227del
ENST00000369856.8:c.6145+2_6146del
ENST00000422373.6:c.3161-324_3161-249del	ENSP00000416926.2:n.3161-324_3161-249del
ENST00000610817.5:c.6283+2_6284del
ENST00000673639.2:c.280-4309_280-4234del
ENST00000676696.1:c.6505+2_6506del
ENST00000678304.1:n.1405+2_1406del
ENST00000344736.8:c.6106+2_6107del
ENST00000360319.8:c.6202+2_6203del
ENST00000369850.7:c.6226+2_6227del
ENST00000369856.7:c.6145+2_6146del
ENST00000415241.1:c.428+2_429del
ENST00000420627.5:c.6182+2_6183del
ENST00000422373.5:c.6202+2_6203del
ENST00000444578.1:c.169+2_170del
ENST00000466325.1:n.367_442del
ENST00000490936.5:n.2215+2_2216del
ENST00000610817.4:c.5844+394_5844+469del	ENSP00000480593.1:n.5844+394_5844+469del
NM_001110556.1:c.6226+2_6227del
NM_001456.3:c.6202+2_6203del
XM_011531127.1:c.6130+2_6131del
XM_011531128.1:c.6106+2_6107del
XM_011531129.1:c.6052+2_6053del
XM_011531130.1:c.6028+2_6029del
XM_011531131.1:c.6025+2_6026del
NM_001110556.2:c.6226+2_6227del
NM_001456.4:c.6202+2_6203del