Canonical Allele Identifier: CA2466656835

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154362433G= , CM000685.2:g.154362433G=	GRCh38
NC_000023.10:g.153590801G= , CM000685.1:g.153590801G=	GRCh37
NC_000023.9:g.153243995G=	NCBI36
NG_011506.1:g.17206C=
NG_011506.2:g.17206C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.2550C=	ENSP00000353467.4:p.Val850=
ENST00000369850.10:c.2550C= MANE Select	ENSP00000358866.3:p.Val850=
ENST00000369856.8:c.2469C=	ENSP00000358872.4:p.Val823=
ENST00000422373.6:c.2550C=	ENSP00000416926.2:p.Val850=
ENST00000610817.5:c.2607C=	ENSP00000480593.2:n.2607C=
ENST00000673639.2:c.279+3003C=
ENST00000676696.1:c.2829C=	ENSP00000503392.1:n.2829C=
ENST00000344736.8:c.2550C=	ENSP00000358863.3:p.Val850=
ENST00000360319.8:c.2550C=	ENSP00000353467.4:p.Val850=
ENST00000369850.7:c.2550C=	ENSP00000358866.3:p.Val850=
ENST00000369856.7:c.2469C=	ENSP00000358872.4:p.Val823=
ENST00000420627.5:c.2506C=	ENSP00000408921.1:n.2506C=
ENST00000422373.5:c.2550C=	ENSP00000416926.1:p.Val850=
ENST00000610817.4:c.2469C=	ENSP00000480593.1:p.Val823=
NM_001110556.1:c.2550C=	NP_001104026.1:p.Val850=
NM_001456.3:c.2550C=	NP_001447.2:p.Val850=
XM_011531127.1:c.2550C=	XP_011529429.1:p.Val850=
XM_011531128.1:c.2550C=	XP_011529430.1:p.Val850=
XM_011531129.1:c.2550C=	XP_011529431.1:p.Val850=
XM_011531130.1:c.2550C=	XP_011529432.1:p.Val850=
XM_011531131.1:c.2349C=	XP_011529433.1:p.Val783=
NM_001110556.2:c.2550C= MANE Select	NP_001104026.1:p.Val850=
NM_001456.4:c.2550C=	NP_001447.2:p.Val850=