Canonical Allele Identifier: CA1242497399

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126963A= , CM000664.2:g.32126963A=	GRCh38
NC_000002.11:g.32352032A= , CM000664.1:g.32352032A=	GRCh37
NC_000002.10:g.32205536A=	NCBI36
NG_008730.1:g.68353A= , LRG_714:g.68353A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*774A=	ENSP00000515816.1:n.*774A=
ENST00000315285.9:c.1114A= MANE Select	ENSP00000320885.3:p.Arg372=
ENST00000621856.2:c.1111A=	ENSP00000482496.2:p.Arg371=
ENST00000642281.1:c.983-9600A=
ENST00000642455.1:c.1015A=	ENSP00000493827.1:p.Arg339=
ENST00000642751.1:c.888A=
ENST00000642999.1:c.856A=	ENSP00000496589.1:p.Arg286=
ENST00000643327.1:c.273A=
ENST00000643334.1:c.694A=
ENST00000644408.1:c.990A=
ENST00000644954.1:c.760A=	ENSP00000494312.1:p.Arg254=
ENST00000645159.1:n.466A=
ENST00000645550.1:n.327A=
ENST00000645671.1:c.564A=
ENST00000645730.1:c.461A=
ENST00000646082.1:c.760A=
ENST00000646571.1:c.1018A=	ENSP00000495015.1:p.Arg340=
ENST00000647007.1:n.806A=
ENST00000647133.1:c.674-1445A=
ENST00000315285.7:c.1114A=	ENSP00000320885.3:p.Arg372=
ENST00000345662.5:c.1018A=	ENSP00000340817.1:p.Arg340=
ENST00000615843.4:c.1114A=	ENSP00000480893.1:p.Arg372=
ENST00000621856.1:c.856A=	ENSP00000482496.1:p.Arg286=
NM_014946.3:c.1114A= , LRG_714t1:c.1114A=	NP_055761.2:p.Arg372=
NM_199436.1:c.1018A=	NP_955468.1:p.Arg340=
XM_005264516.3:c.1111A=	XP_005264573.1:p.Arg371=
XM_011533067.1:c.1114A=	XP_011531369.1:p.Arg372=
NM_001363823.1:c.1111A=	NP_001350752.1:p.Arg371=
NM_001363875.1:c.1015A=	NP_001350804.1:p.Arg339=
XM_005264516.5:c.1111A=	XP_005264573.1:p.Arg371=
XM_011533067.2:c.1114A=	XP_011531369.1:p.Arg372=
XM_017004778.2:c.1018A=	XP_016860267.1:p.Arg340=
NM_001363823.2:c.1111A=	NP_001350752.1:p.Arg371=
NM_001363875.2:c.1015A=	NP_001350804.1:p.Arg339=
NM_001377959.1:c.1018A=	NP_001364888.1:p.Arg340=
NM_014946.4:c.1114A= MANE Select	NP_055761.2:p.Arg372=
NM_199436.2:c.1018A=	NP_955468.1:p.Arg340=