Canonical Allele Identifier: CA1242492106

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32116180G= , CM000664.2:g.32116180G=	GRCh38
NC_000002.11:g.32341249G= , CM000664.1:g.32341249G=	GRCh37
NC_000002.10:g.32194753G=	NCBI36
NG_008730.1:g.57570G= , LRG_714:g.57570G=

Transcript Alleles

HGVS	Amino-acid Change
NM_014946.4:c.1066G= MANE Select	NP_055761.2:p.Glu356=
ENST00000315285.9:c.1066G= MANE Select	ENSP00000320885.3:p.Glu356=
NM_001363823.1:c.1063G=	NP_001350752.1:p.Glu355=
NM_001363823.2:c.1063G=	NP_001350752.1:p.Glu355=
NM_001363875.1:c.967G=	NP_001350804.1:p.Glu323=
NM_001363875.2:c.967G=	NP_001350804.1:p.Glu323=
NM_001377959.1:c.970G=	NP_001364888.1:p.Glu324=
NM_014946.3:c.1066G= , LRG_714t1:c.1066G=	NP_055761.2:p.Glu356=
NM_199436.1:c.970G=	NP_955468.1:p.Glu324=
NM_199436.2:c.970G=	NP_955468.1:p.Glu324=
ENST00000315285.7:c.1066G=	ENSP00000320885.3:p.Glu356=
ENST00000345662.5:c.970G=	ENSP00000340817.1:p.Glu324=
ENST00000615843.4:c.1066G=	ENSP00000480893.1:p.Glu356=
ENST00000621856.1:c.808G=	ENSP00000482496.1:p.Glu270=
ENST00000621856.2:c.1063G=	ENSP00000482496.2:p.Glu355=
ENST00000642281.1:c.950G=
ENST00000642455.1:c.967G=	ENSP00000493827.1:p.Glu323=
ENST00000642751.1:c.840G=
ENST00000642999.1:c.808G=	ENSP00000496589.1:p.Glu270=
ENST00000643327.1:c.225G=
ENST00000643334.1:c.646G=
ENST00000644408.1:c.942G=
ENST00000644954.1:c.712G=	ENSP00000494312.1:p.Glu238=
ENST00000645671.1:c.516G=
ENST00000645730.1:c.413G=
ENST00000646082.1:c.712G=
ENST00000646571.1:c.970G=	ENSP00000495015.1:p.Glu324=
ENST00000647007.1:n.758G=
ENST00000647133.1:c.641G=
ENST00000704289.1:c.*726G=	ENSP00000515816.1:n.*726G=
XM_005264516.3:c.1063G=	XP_005264573.1:p.Glu355=
XM_005264516.5:c.1063G=	XP_005264573.1:p.Glu355=
XM_011533067.1:c.1066G=	XP_011531369.1:p.Glu356=
XM_011533067.2:c.1066G=	XP_011531369.1:p.Glu356=
XM_017004778.2:c.970G=	XP_016860267.1:p.Glu324=