Canonical Allele Identifier: CA1242461664

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32063966G= , CM000664.2:g.32063966G=	GRCh38
NC_000002.11:g.32289035G= , CM000664.1:g.32289035G=	GRCh37
NC_000002.10:g.32142539G=	NCBI36
NG_008730.1:g.5356G= , LRG_714:g.5356G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.135G=	ENSP00000515816.1:p.Pro45=
ENST00000315285.9:c.135G= MANE Select	ENSP00000320885.3:p.Pro45=
ENST00000621856.2:c.135G=	ENSP00000482496.2:p.Pro45=
ENST00000642281.1:c.19G=
ENST00000642455.1:c.135G=	ENSP00000493827.1:p.Pro45=
ENST00000642751.1:c.5G=
ENST00000644408.1:c.11G=
ENST00000646571.1:c.135G=	ENSP00000495015.1:p.Pro45=
ENST00000315285.7:c.135G=	ENSP00000320885.3:p.Pro45=
ENST00000345662.5:c.135G=	ENSP00000340817.1:p.Pro45=
ENST00000615843.4:c.135G=	ENSP00000480893.1:p.Pro45=
NM_014946.3:c.135G= , LRG_714t1:c.135G=	NP_055761.2:p.Pro45=
NM_199436.1:c.135G=	NP_955468.1:p.Pro45=
XM_005264516.3:c.135G=	XP_005264573.1:p.Pro45=
XM_011533067.1:c.135G=	XP_011531369.1:p.Pro45=
NM_001363823.1:c.135G=	NP_001350752.1:p.Pro45=
NM_001363875.1:c.135G=	NP_001350804.1:p.Pro45=
XM_005264516.5:c.135G=	XP_005264573.1:p.Pro45=
XM_011533067.2:c.135G=	XP_011531369.1:p.Pro45=
XM_017004778.2:c.135G=	XP_016860267.1:p.Pro45=
NM_001363823.2:c.135G=	NP_001350752.1:p.Pro45=
NM_001363875.2:c.135G=	NP_001350804.1:p.Pro45=
NM_001377959.1:c.135G=	NP_001364888.1:p.Pro45=
NM_014946.4:c.135G= MANE Select	NP_055761.2:p.Pro45=
NM_199436.2:c.135G=	NP_955468.1:p.Pro45=