Canonical Allele Identifier: CA873335214

Gene: FLNA

Linked Data

• dbSNP Id: rs1158569318
• MyVariant Identifiers: chrX:g.154350850_154350851insACTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350851_154350854dup , CM000685.2:g.154350851_154350854dup	GRCh38
NC_000023.10:g.153579219_153579222dup , CM000685.1:g.153579219_153579222dup	GRCh37
NC_000023.9:g.153232413_153232416dup	NCBI36
NG_011506.1:g.28785_28788dup
NG_011506.2:g.28785_28788dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7132+55_7132+58dup	ENSP00000353467.4:n.7132+55_7132+58dup
ENST00000369850.10:c.7156+55_7156+58dup MANE Select	ENSP00000358866.3:n.7156+55_7156+58dup
ENST00000369856.8:c.7075+55_7075+58dup	ENSP00000358872.4:n.7075+55_7075+58dup
ENST00000422373.6:c.3937+55_3937+58dup	ENSP00000416926.2:n.3937+55_3937+58dup
ENST00000610817.5:c.7213+55_7213+58dup	ENSP00000480593.2:n.7213+55_7213+58dup
ENST00000673639.2:c.280-2164_280-2161dup
ENST00000676696.1:c.7435+55_7435+58dup	ENSP00000503392.1:n.7435+55_7435+58dup
ENST00000678304.1:n.2874+55_2874+58dup
ENST00000344736.8:c.7036+55_7036+58dup	ENSP00000358863.3:n.7036+55_7036+58dup
ENST00000360319.8:c.7132+55_7132+58dup	ENSP00000353467.4:n.7132+55_7132+58dup
ENST00000369850.7:c.7156+55_7156+58dup	ENSP00000358866.3:n.7156+55_7156+58dup
ENST00000369856.7:c.7075+55_7075+58dup	ENSP00000358872.4:n.7075+55_7075+58dup
ENST00000420627.5:c.7112+55_7112+58dup	ENSP00000408921.1:n.7112+55_7112+58dup
ENST00000422373.5:c.7132+55_7132+58dup	ENSP00000416926.1:n.7132+55_7132+58dup
ENST00000490936.5:n.3739_3742dup
ENST00000498411.1:n.67+1963_67+1966dup
ENST00000498491.5:n.197+55_197+58dup
ENST00000610817.4:c.6160+55_6160+58dup	ENSP00000480593.1:n.6160+55_6160+58dup
NM_001110556.1:c.7156+55_7156+58dup	NP_001104026.1:n.7156+55_7156+58dup
NM_001456.3:c.7132+55_7132+58dup	NP_001447.2:n.7132+55_7132+58dup
XM_011531127.1:c.7060+55_7060+58dup	XP_011529429.1:n.7060+55_7060+58dup
XM_011531128.1:c.7036+55_7036+58dup	XP_011529430.1:n.7036+55_7036+58dup
XM_011531129.1:c.6982+55_6982+58dup	XP_011529431.1:n.6982+55_6982+58dup
XM_011531130.1:c.6958+55_6958+58dup	XP_011529432.1:n.6958+55_6958+58dup
XM_011531131.1:c.6955+55_6955+58dup	XP_011529433.1:n.6955+55_6955+58dup
NM_001110556.2:c.7156+55_7156+58dup MANE Select	NP_001104026.1:n.7156+55_7156+58dup
NM_001456.4:c.7132+55_7132+58dup	NP_001447.2:n.7132+55_7132+58dup