Canonical Allele Identifier: CA2695237747

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154359240_154359247del , CM000685.2:g.154359240_154359247del	GRCh38
NC_000023.10:g.153587608_153587615del , CM000685.1:g.153587608_153587615del	GRCh37
NC_000023.9:g.153240802_153240809del	NCBI36
NG_011506.1:g.20397_20404del
NG_011506.2:g.20397_20404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.4303+4_4303+11del
ENST00000369850.10:c.4303+4_4303+11del
ENST00000369856.8:c.4222+4_4222+11del
ENST00000422373.6:c.3160+2113_3160+2120del	ENSP00000416926.2:n.3160+2113_3160+2120del
ENST00000610817.5:c.4360+4_4360+11del
ENST00000673639.2:c.279+6194_279+6201del
ENST00000676696.1:c.4582+4_4582+11del
ENST00000678304.1:n.82+4_82+11del
ENST00000344736.8:c.4303+4_4303+11del
ENST00000360319.8:c.4303+4_4303+11del
ENST00000369850.7:c.4303+4_4303+11del
ENST00000369856.7:c.4222+4_4222+11del
ENST00000420627.5:c.4259+4_4259+11del
ENST00000422373.5:c.4303+4_4303+11del
ENST00000490936.5:n.316+4_316+11del
ENST00000610817.4:c.4222+4_4222+11del
NM_001110556.1:c.4303+4_4303+11del
NM_001456.3:c.4303+4_4303+11del
XM_011531127.1:c.4303+4_4303+11del
XM_011531128.1:c.4303+4_4303+11del
XM_011531129.1:c.4303+4_4303+11del
XM_011531130.1:c.4303+4_4303+11del
XM_011531131.1:c.4102+4_4102+11del
NM_001110556.2:c.4303+4_4303+11del
NM_001456.4:c.4303+4_4303+11del