Canonical Allele Identifier: CA1242497428

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32127014A= , CM000664.2:g.32127014A=	GRCh38
NC_000002.11:g.32352083A= , CM000664.1:g.32352083A=	GRCh37
NC_000002.10:g.32205587A=	NCBI36
NG_008730.1:g.68404A= , LRG_714:g.68404A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*825A=	ENSP00000515816.1:n.*825A=
ENST00000315285.9:c.1165A= MANE Select	ENSP00000320885.3:p.Thr389=
ENST00000621856.2:c.1162A=	ENSP00000482496.2:p.Thr388=
ENST00000642281.1:c.983-9549A=
ENST00000642455.1:c.1066A=	ENSP00000493827.1:p.Thr356=
ENST00000642751.1:c.939A=
ENST00000642999.1:c.907A=	ENSP00000496589.1:p.Thr303=
ENST00000643327.1:c.324A=
ENST00000643334.1:c.745A=
ENST00000644408.1:c.1041A=
ENST00000644954.1:c.811A=	ENSP00000494312.1:p.Thr271=
ENST00000645159.1:n.517A=
ENST00000645550.1:n.378A=
ENST00000645671.1:c.615A=
ENST00000645730.1:c.512A=
ENST00000646082.1:c.811A=
ENST00000646571.1:c.1069A=	ENSP00000495015.1:p.Thr357=
ENST00000647007.1:n.857A=
ENST00000647133.1:c.674-1394A=
ENST00000315285.7:c.1165A=	ENSP00000320885.3:p.Thr389=
ENST00000345662.5:c.1069A=	ENSP00000340817.1:p.Thr357=
ENST00000615843.4:c.1165A=	ENSP00000480893.1:p.Thr389=
ENST00000621856.1:c.907A=	ENSP00000482496.1:p.Thr303=
NM_014946.3:c.1165A= , LRG_714t1:c.1165A=	NP_055761.2:p.Thr389=
NM_199436.1:c.1069A=	NP_955468.1:p.Thr357=
XM_005264516.3:c.1162A=	XP_005264573.1:p.Thr388=
XM_011533067.1:c.1165A=	XP_011531369.1:p.Thr389=
NM_001363823.1:c.1162A=	NP_001350752.1:p.Thr388=
NM_001363875.1:c.1066A=	NP_001350804.1:p.Thr356=
XM_005264516.5:c.1162A=	XP_005264573.1:p.Thr388=
XM_011533067.2:c.1165A=	XP_011531369.1:p.Thr389=
XM_017004778.2:c.1069A=	XP_016860267.1:p.Thr357=
NM_001363823.2:c.1162A=	NP_001350752.1:p.Thr388=
NM_001363875.2:c.1066A=	NP_001350804.1:p.Thr356=
NM_001377959.1:c.1069A=	NP_001364888.1:p.Thr357=
NM_014946.4:c.1165A= MANE Select	NP_055761.2:p.Thr389=
NM_199436.2:c.1069A=	NP_955468.1:p.Thr357=