Canonical Allele Identifier: CA1242491896

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32115756C= , CM000664.2:g.32115756C=	GRCh38
NC_000002.11:g.32340825C= , CM000664.1:g.32340825C=	GRCh37
NC_000002.10:g.32194329C=	NCBI36
NG_008730.1:g.57146C= , LRG_714:g.57146C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*585C=	ENSP00000515816.1:n.*585C=
ENST00000315285.9:c.925C= MANE Select	ENSP00000320885.3:p.Arg309=
ENST00000621856.2:c.922C=	ENSP00000482496.2:p.Arg308=
ENST00000642281.1:c.809C=
ENST00000642455.1:c.826C=	ENSP00000493827.1:p.Arg276=
ENST00000642751.1:c.699C=
ENST00000642999.1:c.667C=	ENSP00000496589.1:p.Arg223=
ENST00000643327.1:c.84C=
ENST00000643334.1:c.505C=
ENST00000644408.1:c.801C=
ENST00000644954.1:c.571C=	ENSP00000494312.1:p.Arg191=
ENST00000645671.1:c.375C=
ENST00000645730.1:c.272C=
ENST00000646082.1:c.571C=
ENST00000646571.1:c.829C=	ENSP00000495015.1:p.Arg277=
ENST00000647007.1:n.617C=
ENST00000647133.1:c.500C=
ENST00000315285.7:c.925C=	ENSP00000320885.3:p.Arg309=
ENST00000345662.5:c.829C=	ENSP00000340817.1:p.Arg277=
ENST00000615843.4:c.925C=	ENSP00000480893.1:p.Arg309=
ENST00000621856.1:c.667C=	ENSP00000482496.1:p.Arg223=
NM_014946.3:c.925C= , LRG_714t1:c.925C=	NP_055761.2:p.Arg309=
NM_199436.1:c.829C=	NP_955468.1:p.Arg277=
XM_005264516.3:c.922C=	XP_005264573.1:p.Arg308=
XM_011533067.1:c.925C=	XP_011531369.1:p.Arg309=
NM_001363823.1:c.922C=	NP_001350752.1:p.Arg308=
NM_001363875.1:c.826C=	NP_001350804.1:p.Arg276=
XM_005264516.5:c.922C=	XP_005264573.1:p.Arg308=
XM_011533067.2:c.925C=	XP_011531369.1:p.Arg309=
XM_017004778.2:c.829C=	XP_016860267.1:p.Arg277=
NM_001363823.2:c.922C=	NP_001350752.1:p.Arg308=
NM_001363875.2:c.826C=	NP_001350804.1:p.Arg276=
NM_001377959.1:c.829C=	NP_001364888.1:p.Arg277=
NM_014946.4:c.925C= MANE Select	NP_055761.2:p.Arg309=
NM_199436.2:c.829C=	NP_955468.1:p.Arg277=