Canonical Allele Identifier: CA519708167

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154359907_154359990del , CM000685.2:g.154359907_154359990del	GRCh38
NC_000023.10:g.153588275_153588358del , CM000685.1:g.153588275_153588358del	GRCh37
NC_000023.9:g.153241469_153241552del	NCBI36
NG_011506.1:g.19653_19736del
NG_011506.2:g.19653_19736del

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.1:c.3805+4_3808del
NM_001110556.2:c.3805+4_3808del
NM_001456.3:c.3805+4_3808del
NM_001456.4:c.3805+4_3808del
ENST00000344736.8:c.3805+4_3808del
ENST00000360319.8:c.3805+4_3808del
ENST00000360319.9:c.3805+4_3808del
ENST00000369850.10:c.3805+4_3808del
ENST00000369850.7:c.3805+4_3808del
ENST00000369856.7:c.3724+4_3727del
ENST00000369856.8:c.3724+4_3727del
ENST00000420627.5:c.3761+4_3764del
ENST00000422373.5:c.3805+4_3808del
ENST00000422373.6:c.3160+1369_3160+1452del	ENSP00000416926.2:n.3160+1369_3160+1452del
ENST00000610817.4:c.3724+4_3727del
ENST00000610817.5:c.3862+4_3865del
ENST00000673639.2:c.279+5450_279+5533del
ENST00000676696.1:c.4084+4_4087del
XM_011531127.1:c.3805+4_3808del
XM_011531128.1:c.3805+4_3808del
XM_011531129.1:c.3805+4_3808del
XM_011531130.1:c.3805+4_3808del
XM_011531131.1:c.3604+4_3607del