Canonical Allele Identifier: CA2695111387

Gene: FLNA

Linked Data

• gnomAD v4: X-154350583-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350584del , CM000685.2:g.154350584del	GRCh38
NC_000023.10:g.153578952del , CM000685.1:g.153578952del	GRCh37
NC_000023.9:g.153232146del	NCBI36
NG_011506.1:g.29055del
NG_011506.2:g.29055del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7132+325del	ENSP00000353467.4:n.7132+325del
ENST00000369850.10:c.7156+325del MANE Select	ENSP00000358866.3:n.7156+325del
ENST00000369856.8:c.7075+325del	ENSP00000358872.4:n.7075+325del
ENST00000422373.6:c.3937+325del	ENSP00000416926.2:n.3937+325del
ENST00000610817.5:c.7213+325del	ENSP00000480593.2:n.7213+325del
ENST00000673639.2:c.280-1894del
ENST00000676696.1:c.7435+325del	ENSP00000503392.1:n.7435+325del
ENST00000678304.1:n.2874+325del
ENST00000344736.8:c.7036+325del	ENSP00000358863.3:n.7036+325del
ENST00000360319.8:c.7132+325del	ENSP00000353467.4:n.7132+325del
ENST00000369850.7:c.7156+325del	ENSP00000358866.3:n.7156+325del
ENST00000369856.7:c.7075+325del	ENSP00000358872.4:n.7075+325del
ENST00000420627.5:c.7112+325del	ENSP00000408921.1:n.7112+325del
ENST00000422373.5:c.7132+325del	ENSP00000416926.1:n.7132+325del
ENST00000490936.5:n.4009del
ENST00000498411.1:n.68-1754del
ENST00000498491.5:n.197+325del
ENST00000610817.4:c.6160+325del	ENSP00000480593.1:n.6160+325del
NM_001110556.1:c.7156+325del	NP_001104026.1:n.7156+325del
NM_001456.3:c.7132+325del	NP_001447.2:n.7132+325del
XM_011531127.1:c.7060+325del	XP_011529429.1:n.7060+325del
XM_011531128.1:c.7036+325del	XP_011529430.1:n.7036+325del
XM_011531129.1:c.6982+325del	XP_011529431.1:n.6982+325del
XM_011531130.1:c.6958+325del	XP_011529432.1:n.6958+325del
XM_011531131.1:c.6955+325del	XP_011529433.1:n.6955+325del
NM_001110556.2:c.7156+325del MANE Select	NP_001104026.1:n.7156+325del
NM_001456.4:c.7132+325del	NP_001447.2:n.7132+325del