Canonical Allele Identifier: CA1242501800

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136967G= , CM000664.2:g.32136967G=	GRCh38
NC_000002.11:g.32362036G= , CM000664.1:g.32362036G=	GRCh37
NC_000002.10:g.32215540G=	NCBI36
NG_008730.1:g.78357G= , LRG_714:g.78357G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1072G=	ENSP00000515816.1:n.*1072G=
ENST00000315285.9:c.1412G= MANE Select	ENSP00000320885.3:p.Gly471=
ENST00000621856.2:c.1409G=	ENSP00000482496.2:p.Gly470=
ENST00000642281.1:c.1149G=
ENST00000642455.1:c.1313G=	ENSP00000493827.1:p.Gly438=
ENST00000642751.1:c.1186G=
ENST00000642999.1:c.1154G=	ENSP00000496589.1:p.Gly385=
ENST00000643327.1:c.481-142G=
ENST00000643334.1:c.992G=
ENST00000644408.1:c.1288G=
ENST00000644954.1:c.1058G=	ENSP00000494312.1:p.Gly353=
ENST00000645159.1:n.2149G=
ENST00000645671.1:c.862G=
ENST00000645730.1:c.593-142G=
ENST00000646082.1:c.1058G=
ENST00000646571.1:c.1316G=	ENSP00000495015.1:p.Gly439=
ENST00000647007.1:n.1104G=
ENST00000647133.1:c.912G=
ENST00000315285.7:c.1412G=	ENSP00000320885.3:p.Gly471=
ENST00000345662.5:c.1316G=	ENSP00000340817.1:p.Gly439=
ENST00000615843.4:c.1412G=	ENSP00000480893.1:p.Gly471=
ENST00000621856.1:c.1154G=	ENSP00000482496.1:p.Gly385=
NM_014946.3:c.1412G= , LRG_714t1:c.1412G=	NP_055761.2:p.Gly471=
NM_199436.1:c.1316G=	NP_955468.1:p.Gly439=
XM_005264516.3:c.1409G=	XP_005264573.1:p.Gly470=
XM_011533067.1:c.1412G=	XP_011531369.1:p.Gly471=
NM_001363823.1:c.1409G=	NP_001350752.1:p.Gly470=
NM_001363875.1:c.1313G=	NP_001350804.1:p.Gly438=
XM_005264516.5:c.1409G=	XP_005264573.1:p.Gly470=
XM_011533067.2:c.1412G=	XP_011531369.1:p.Gly471=
XM_017004778.2:c.1316G=	XP_016860267.1:p.Gly439=
NM_001363823.2:c.1409G=	NP_001350752.1:p.Gly470=
NM_001363875.2:c.1313G=	NP_001350804.1:p.Gly438=
NM_001377959.1:c.1316G=	NP_001364888.1:p.Gly439=
NM_014946.4:c.1412G= MANE Select	NP_055761.2:p.Gly471=
NM_199436.2:c.1316G=	NP_955468.1:p.Gly439=