Canonical Allele Identifier: CA1242502027

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32137127G= , CM000664.2:g.32137127G=	GRCh38
NC_000002.11:g.32362196G= , CM000664.1:g.32362196G=	GRCh37
NC_000002.10:g.32215700G=	NCBI36
NG_008730.1:g.78517G= , LRG_714:g.78517G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1092G=	ENSP00000515816.1:n.*1092G=
ENST00000315285.9:c.1432G= MANE Select	ENSP00000320885.3:p.Asp478=
ENST00000621856.2:c.1429G=	ENSP00000482496.2:p.Asp477=
ENST00000642281.1:c.1169G=
ENST00000642455.1:c.1333G=	ENSP00000493827.1:p.Asp445=
ENST00000642751.1:c.1206G=
ENST00000642999.1:c.1174G=	ENSP00000496589.1:p.Asp392=
ENST00000643327.1:c.499G=
ENST00000643334.1:c.1012G=
ENST00000644408.1:c.1308G=
ENST00000644954.1:c.1078G=	ENSP00000494312.1:p.Asp360=
ENST00000645159.1:n.2169G=
ENST00000645671.1:c.882G=
ENST00000645730.1:c.611G=
ENST00000646082.1:c.1078G=
ENST00000646571.1:c.1336G=	ENSP00000495015.1:p.Asp446=
ENST00000647007.1:n.1124G=
ENST00000647133.1:c.932G=
ENST00000315285.7:c.1432G=	ENSP00000320885.3:p.Asp478=
ENST00000345662.5:c.1336G=	ENSP00000340817.1:p.Asp446=
ENST00000615843.4:c.1432G=	ENSP00000480893.1:p.Asp478=
ENST00000621856.1:c.1174G=	ENSP00000482496.1:p.Asp392=
NM_014946.3:c.1432G= , LRG_714t1:c.1432G=	NP_055761.2:p.Asp478=
NM_199436.1:c.1336G=	NP_955468.1:p.Asp446=
XM_005264516.3:c.1429G=	XP_005264573.1:p.Asp477=
XM_011533067.1:c.1432G=	XP_011531369.1:p.Asp478=
NM_001363823.1:c.1429G=	NP_001350752.1:p.Asp477=
NM_001363875.1:c.1333G=	NP_001350804.1:p.Asp445=
XM_005264516.5:c.1429G=	XP_005264573.1:p.Asp477=
XM_011533067.2:c.1432G=	XP_011531369.1:p.Asp478=
XM_017004778.2:c.1336G=	XP_016860267.1:p.Asp446=
NM_001363823.2:c.1429G=	NP_001350752.1:p.Asp477=
NM_001363875.2:c.1333G=	NP_001350804.1:p.Asp445=
NM_001377959.1:c.1336G=	NP_001364888.1:p.Asp446=
NM_014946.4:c.1432G= MANE Select	NP_055761.2:p.Asp478=
NM_199436.2:c.1336G=	NP_955468.1:p.Asp446=