Canonical Allele Identifier: CA1242497422

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32127006A= , CM000664.2:g.32127006A=	GRCh38
NC_000002.11:g.32352075A= , CM000664.1:g.32352075A=	GRCh37
NC_000002.10:g.32205579A=	NCBI36
NG_008730.1:g.68396A= , LRG_714:g.68396A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*817A=	ENSP00000515816.1:n.*817A=
ENST00000315285.9:c.1157A= MANE Select	ENSP00000320885.3:p.Asn386=
ENST00000621856.2:c.1154A=	ENSP00000482496.2:p.Asn385=
ENST00000642281.1:c.983-9557A=
ENST00000642455.1:c.1058A=	ENSP00000493827.1:p.Asn353=
ENST00000642751.1:c.931A=
ENST00000642999.1:c.899A=	ENSP00000496589.1:p.Asn300=
ENST00000643327.1:c.316A=
ENST00000643334.1:c.737A=
ENST00000644408.1:c.1033A=
ENST00000644954.1:c.803A=	ENSP00000494312.1:p.Asn268=
ENST00000645159.1:n.509A=
ENST00000645550.1:n.370A=
ENST00000645671.1:c.607A=
ENST00000645730.1:c.504A=
ENST00000646082.1:c.803A=
ENST00000646571.1:c.1061A=	ENSP00000495015.1:p.Asn354=
ENST00000647007.1:n.849A=
ENST00000647133.1:c.674-1402A=
ENST00000315285.7:c.1157A=	ENSP00000320885.3:p.Asn386=
ENST00000345662.5:c.1061A=	ENSP00000340817.1:p.Asn354=
ENST00000615843.4:c.1157A=	ENSP00000480893.1:p.Asn386=
ENST00000621856.1:c.899A=	ENSP00000482496.1:p.Asn300=
NM_014946.3:c.1157A= , LRG_714t1:c.1157A=	NP_055761.2:p.Asn386=
NM_199436.1:c.1061A=	NP_955468.1:p.Asn354=
XM_005264516.3:c.1154A=	XP_005264573.1:p.Asn385=
XM_011533067.1:c.1157A=	XP_011531369.1:p.Asn386=
NM_001363823.1:c.1154A=	NP_001350752.1:p.Asn385=
NM_001363875.1:c.1058A=	NP_001350804.1:p.Asn353=
XM_005264516.5:c.1154A=	XP_005264573.1:p.Asn385=
XM_011533067.2:c.1157A=	XP_011531369.1:p.Asn386=
XM_017004778.2:c.1061A=	XP_016860267.1:p.Asn354=
NM_001363823.2:c.1154A=	NP_001350752.1:p.Asn385=
NM_001363875.2:c.1058A=	NP_001350804.1:p.Asn353=
NM_001377959.1:c.1061A=	NP_001364888.1:p.Asn354=
NM_014946.4:c.1157A= MANE Select	NP_055761.2:p.Asn386=
NM_199436.2:c.1061A=	NP_955468.1:p.Asn354=