Canonical Allele Identifier: CA1242497411

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126987C= , CM000664.2:g.32126987C=	GRCh38
NC_000002.11:g.32352056C= , CM000664.1:g.32352056C=	GRCh37
NC_000002.10:g.32205560C=	NCBI36
NG_008730.1:g.68377C= , LRG_714:g.68377C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*798C=	ENSP00000515816.1:n.*798C=
ENST00000315285.9:c.1138C= MANE Select	ENSP00000320885.3:p.Leu380=
ENST00000621856.2:c.1135C=	ENSP00000482496.2:p.Leu379=
ENST00000642281.1:c.983-9576C=
ENST00000642455.1:c.1039C=	ENSP00000493827.1:p.Leu347=
ENST00000642751.1:c.912C=
ENST00000642999.1:c.880C=	ENSP00000496589.1:p.Leu294=
ENST00000643327.1:c.297C=
ENST00000643334.1:c.718C=
ENST00000644408.1:c.1014C=
ENST00000644954.1:c.784C=	ENSP00000494312.1:p.Leu262=
ENST00000645159.1:n.490C=
ENST00000645550.1:n.351C=
ENST00000645671.1:c.588C=
ENST00000645730.1:c.485C=
ENST00000646082.1:c.784C=
ENST00000646571.1:c.1042C=	ENSP00000495015.1:p.Leu348=
ENST00000647007.1:n.830C=
ENST00000647133.1:c.674-1421C=
ENST00000315285.7:c.1138C=	ENSP00000320885.3:p.Leu380=
ENST00000345662.5:c.1042C=	ENSP00000340817.1:p.Leu348=
ENST00000615843.4:c.1138C=	ENSP00000480893.1:p.Leu380=
ENST00000621856.1:c.880C=	ENSP00000482496.1:p.Leu294=
NM_014946.3:c.1138C= , LRG_714t1:c.1138C=	NP_055761.2:p.Leu380=
NM_199436.1:c.1042C=	NP_955468.1:p.Leu348=
XM_005264516.3:c.1135C=	XP_005264573.1:p.Leu379=
XM_011533067.1:c.1138C=	XP_011531369.1:p.Leu380=
NM_001363823.1:c.1135C=	NP_001350752.1:p.Leu379=
NM_001363875.1:c.1039C=	NP_001350804.1:p.Leu347=
XM_005264516.5:c.1135C=	XP_005264573.1:p.Leu379=
XM_011533067.2:c.1138C=	XP_011531369.1:p.Leu380=
XM_017004778.2:c.1042C=	XP_016860267.1:p.Leu348=
NM_001363823.2:c.1135C=	NP_001350752.1:p.Leu379=
NM_001363875.2:c.1039C=	NP_001350804.1:p.Leu347=
NM_001377959.1:c.1042C=	NP_001364888.1:p.Leu348=
NM_014946.4:c.1138C= MANE Select	NP_055761.2:p.Leu380=
NM_199436.2:c.1042C=	NP_955468.1:p.Leu348=