Canonical Allele Identifier: CA2466652252

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350618A= , CM000685.2:g.154350618A=	GRCh38
NC_000023.10:g.153578986A= , CM000685.1:g.153578986A=	GRCh37
NC_000023.9:g.153232180A=	NCBI36
NG_011506.1:g.29021T=
NG_011506.2:g.29021T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7132+291T=	ENSP00000353467.4:n.7132+291T=
ENST00000369850.10:c.7156+291T= MANE Select	ENSP00000358866.3:n.7156+291T=
ENST00000369856.8:c.7075+291T=	ENSP00000358872.4:n.7075+291T=
ENST00000422373.6:c.3937+291T=	ENSP00000416926.2:n.3937+291T=
ENST00000610817.5:c.7213+291T=	ENSP00000480593.2:n.7213+291T=
ENST00000673639.2:c.280-1928T=
ENST00000676696.1:c.7435+291T=	ENSP00000503392.1:n.7435+291T=
ENST00000678304.1:n.2874+291T=
ENST00000344736.8:c.7036+291T=	ENSP00000358863.3:n.7036+291T=
ENST00000360319.8:c.7132+291T=	ENSP00000353467.4:n.7132+291T=
ENST00000369850.7:c.7156+291T=	ENSP00000358866.3:n.7156+291T=
ENST00000369856.7:c.7075+291T=	ENSP00000358872.4:n.7075+291T=
ENST00000420627.5:c.7112+291T=	ENSP00000408921.1:n.7112+291T=
ENST00000422373.5:c.7132+291T=	ENSP00000416926.1:n.7132+291T=
ENST00000490936.5:n.3975T=
ENST00000498411.1:n.68-1788T=
ENST00000498491.5:n.197+291T=
ENST00000610817.4:c.6160+291T=	ENSP00000480593.1:n.6160+291T=
NM_001110556.1:c.7156+291T=	NP_001104026.1:n.7156+291T=
NM_001456.3:c.7132+291T=	NP_001447.2:n.7132+291T=
XM_011531127.1:c.7060+291T=	XP_011529429.1:n.7060+291T=
XM_011531128.1:c.7036+291T=	XP_011529430.1:n.7036+291T=
XM_011531129.1:c.6982+291T=	XP_011529431.1:n.6982+291T=
XM_011531130.1:c.6958+291T=	XP_011529432.1:n.6958+291T=
XM_011531131.1:c.6955+291T=	XP_011529433.1:n.6955+291T=
NM_001110556.2:c.7156+291T= MANE Select	NP_001104026.1:n.7156+291T=
NM_001456.4:c.7132+291T=	NP_001447.2:n.7132+291T=