Canonical Allele Identifier: CA1242498115

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128408G= , CM000664.2:g.32128408G=	GRCh38
NC_000002.11:g.32353477G= , CM000664.1:g.32353477G=	GRCh37
NC_000002.10:g.32206981G=	NCBI36
NG_008730.1:g.69798G= , LRG_714:g.69798G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*834G=	ENSP00000515816.1:n.*834G=
ENST00000315285.9:c.1174G= MANE Select	ENSP00000320885.3:p.Ala392=
ENST00000621856.2:c.1171G=	ENSP00000482496.2:p.Ala391=
ENST00000642281.1:c.983-8155G=
ENST00000642455.1:c.1075G=	ENSP00000493827.1:p.Ala359=
ENST00000642751.1:c.948G=
ENST00000642999.1:c.916G=	ENSP00000496589.1:p.Ala306=
ENST00000643327.1:c.333G=
ENST00000643334.1:c.754G=
ENST00000644408.1:c.1050G=
ENST00000644954.1:c.820G=	ENSP00000494312.1:p.Ala274=
ENST00000645159.1:n.1911G=
ENST00000645550.1:n.387G=
ENST00000645671.1:c.624G=
ENST00000645730.1:c.521G=
ENST00000646082.1:c.820G=
ENST00000646571.1:c.1078G=	ENSP00000495015.1:p.Ala360=
ENST00000647007.1:n.866G=
ENST00000647133.1:c.674G=
ENST00000315285.7:c.1174G=	ENSP00000320885.3:p.Ala392=
ENST00000345662.5:c.1078G=	ENSP00000340817.1:p.Ala360=
ENST00000615843.4:c.1174G=	ENSP00000480893.1:p.Ala392=
ENST00000621856.1:c.916G=	ENSP00000482496.1:p.Ala306=
NM_014946.3:c.1174G= , LRG_714t1:c.1174G=	NP_055761.2:p.Ala392=
NM_199436.1:c.1078G=	NP_955468.1:p.Ala360=
XM_005264516.3:c.1171G=	XP_005264573.1:p.Ala391=
XM_011533067.1:c.1174G=	XP_011531369.1:p.Ala392=
NM_001363823.1:c.1171G=	NP_001350752.1:p.Ala391=
NM_001363875.1:c.1075G=	NP_001350804.1:p.Ala359=
XM_005264516.5:c.1171G=	XP_005264573.1:p.Ala391=
XM_011533067.2:c.1174G=	XP_011531369.1:p.Ala392=
XM_017004778.2:c.1078G=	XP_016860267.1:p.Ala360=
NM_001363823.2:c.1171G=	NP_001350752.1:p.Ala391=
NM_001363875.2:c.1075G=	NP_001350804.1:p.Ala359=
NM_001377959.1:c.1078G=	NP_001364888.1:p.Ala360=
NM_014946.4:c.1174G= MANE Select	NP_055761.2:p.Ala392=
NM_199436.2:c.1078G=	NP_955468.1:p.Ala360=