Canonical Allele Identifier: CA1242492115

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32116199C= , CM000664.2:g.32116199C=	GRCh38
NC_000002.11:g.32341268C= , CM000664.1:g.32341268C=	GRCh37
NC_000002.10:g.32194772C=	NCBI36
NG_008730.1:g.57589C= , LRG_714:g.57589C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*745C=	ENSP00000515816.1:n.*745C=
ENST00000315285.9:c.1085C= MANE Select	ENSP00000320885.3:p.Ser362=
ENST00000621856.2:c.1082C=	ENSP00000482496.2:p.Ser361=
ENST00000642281.1:c.969C=
ENST00000642455.1:c.986C=	ENSP00000493827.1:p.Ser329=
ENST00000642751.1:c.859C=
ENST00000642999.1:c.827C=	ENSP00000496589.1:p.Ser276=
ENST00000643327.1:c.244C=
ENST00000643334.1:c.665C=
ENST00000644408.1:c.961C=
ENST00000644954.1:c.731C=	ENSP00000494312.1:p.Ser244=
ENST00000645671.1:c.535C=
ENST00000645730.1:c.432C=
ENST00000646082.1:c.731C=
ENST00000646571.1:c.989C=	ENSP00000495015.1:p.Ser330=
ENST00000647007.1:n.777C=
ENST00000647133.1:c.660C=
ENST00000315285.7:c.1085C=	ENSP00000320885.3:p.Ser362=
ENST00000345662.5:c.989C=	ENSP00000340817.1:p.Ser330=
ENST00000615843.4:c.1085C=	ENSP00000480893.1:p.Ser362=
ENST00000621856.1:c.827C=	ENSP00000482496.1:p.Ser276=
NM_014946.3:c.1085C= , LRG_714t1:c.1085C=	NP_055761.2:p.Ser362=
NM_199436.1:c.989C=	NP_955468.1:p.Ser330=
XM_005264516.3:c.1082C=	XP_005264573.1:p.Ser361=
XM_011533067.1:c.1085C=	XP_011531369.1:p.Ser362=
NM_001363823.1:c.1082C=	NP_001350752.1:p.Ser361=
NM_001363875.1:c.986C=	NP_001350804.1:p.Ser329=
XM_005264516.5:c.1082C=	XP_005264573.1:p.Ser361=
XM_011533067.2:c.1085C=	XP_011531369.1:p.Ser362=
XM_017004778.2:c.989C=	XP_016860267.1:p.Ser330=
NM_001363823.2:c.1082C=	NP_001350752.1:p.Ser361=
NM_001363875.2:c.986C=	NP_001350804.1:p.Ser329=
NM_001377959.1:c.989C=	NP_001364888.1:p.Ser330=
NM_014946.4:c.1085C= MANE Select	NP_055761.2:p.Ser362=
NM_199436.2:c.989C=	NP_955468.1:p.Ser330=