Canonical Allele Identifier: CA1242504519

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32141917C= , CM000664.2:g.32141917C=	GRCh38
NC_000002.11:g.32366986C= , CM000664.1:g.32366986C=	GRCh37
NC_000002.10:g.32220490C=	NCBI36
NG_008730.1:g.83307C= , LRG_714:g.83307C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1167C=	ENSP00000515816.1:n.*1167C=
ENST00000315285.9:c.1507C= MANE Select	ENSP00000320885.3:p.Arg503=
ENST00000621856.2:c.1504C=	ENSP00000482496.2:p.Arg502=
ENST00000642281.1:c.1244C=
ENST00000642455.1:c.1408C=	ENSP00000493827.1:p.Arg470=
ENST00000642751.1:c.1281C=
ENST00000642999.1:c.1249C=	ENSP00000496589.1:p.Arg417=
ENST00000643327.1:c.574C=
ENST00000643334.1:c.1087C=
ENST00000644408.1:c.1383C=
ENST00000644954.1:c.1153C=	ENSP00000494312.1:p.Arg385=
ENST00000645159.1:n.2244C=
ENST00000645671.1:c.957C=
ENST00000645730.1:c.686C=
ENST00000646082.1:c.1153C=
ENST00000646571.1:c.1411C=	ENSP00000495015.1:p.Arg471=
ENST00000647007.1:n.1199C=
ENST00000647133.1:c.1007C=
ENST00000315285.7:c.1507C=	ENSP00000320885.3:p.Arg503=
ENST00000345662.5:c.1411C=	ENSP00000340817.1:p.Arg471=
ENST00000615843.4:c.1507C=	ENSP00000480893.1:p.Arg503=
ENST00000621856.1:c.1249C=	ENSP00000482496.1:p.Arg417=
NM_014946.3:c.1507C= , LRG_714t1:c.1507C=	NP_055761.2:p.Arg503=
NM_199436.1:c.1411C=	NP_955468.1:p.Arg471=
XM_005264516.3:c.1504C=	XP_005264573.1:p.Arg502=
XM_011533067.1:c.1507C=	XP_011531369.1:p.Arg503=
NM_001363823.1:c.1504C=	NP_001350752.1:p.Arg502=
NM_001363875.1:c.1408C=	NP_001350804.1:p.Arg470=
XM_005264516.5:c.1504C=	XP_005264573.1:p.Arg502=
XM_011533067.2:c.1507C=	XP_011531369.1:p.Arg503=
XM_017004778.2:c.1411C=	XP_016860267.1:p.Arg471=
NM_001363823.2:c.1504C=	NP_001350752.1:p.Arg502=
NM_001363875.2:c.1408C=	NP_001350804.1:p.Arg470=
NM_001377959.1:c.1411C=	NP_001364888.1:p.Arg471=
NM_014946.4:c.1507C= MANE Select	NP_055761.2:p.Arg503=
NM_199436.2:c.1411C=	NP_955468.1:p.Arg471=