Canonical Allele Identifier: CA2579738012

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154358958del , CM000685.2:g.154358958del	GRCh38
NC_000023.10:g.153587326del , CM000685.1:g.153587326del	GRCh37
NC_000023.9:g.153240520del	NCBI36
NG_011506.1:g.20684del
NG_011506.2:g.20684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.4474+29del	ENSP00000353467.4:n.4474+29del
ENST00000369850.10:c.4474+29del MANE Select	ENSP00000358866.3:n.4474+29del
ENST00000369856.8:c.4393+29del	ENSP00000358872.4:n.4393+29del
ENST00000422373.6:c.3160+2400del	ENSP00000416926.2:n.3160+2400del
ENST00000610817.5:c.4531+29del	ENSP00000480593.2:n.4531+29del
ENST00000673639.2:c.279+6481del
ENST00000676696.1:c.4753+29del	ENSP00000503392.1:n.4753+29del
ENST00000678304.1:n.148+134del
ENST00000344736.8:c.4474+29del	ENSP00000358863.3:n.4474+29del
ENST00000360319.8:c.4474+29del	ENSP00000353467.4:n.4474+29del
ENST00000369850.7:c.4474+29del	ENSP00000358866.3:n.4474+29del
ENST00000369856.7:c.4393+29del	ENSP00000358872.4:n.4393+29del
ENST00000420627.5:c.4430+29del	ENSP00000408921.1:n.4430+29del
ENST00000422373.5:c.4474+29del	ENSP00000416926.1:n.4474+29del
ENST00000490936.5:n.487+29del
ENST00000610817.4:c.4393+29del	ENSP00000480593.1:n.4393+29del
NM_001110556.1:c.4474+29del	NP_001104026.1:n.4474+29del
NM_001456.3:c.4474+29del	NP_001447.2:n.4474+29del
XM_011531127.1:c.4474+29del	XP_011529429.1:n.4474+29del
XM_011531128.1:c.4474+29del	XP_011529430.1:n.4474+29del
XM_011531129.1:c.4474+29del	XP_011529431.1:n.4474+29del
XM_011531130.1:c.4474+29del	XP_011529432.1:n.4474+29del
XM_011531131.1:c.4273+29del	XP_011529433.1:n.4273+29del
NM_001110556.2:c.4474+29del MANE Select	NP_001104026.1:n.4474+29del
NM_001456.4:c.4474+29del	NP_001447.2:n.4474+29del