Canonical Allele Identifier: CA1242498090

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128350T= , CM000664.2:g.32128350T=	GRCh38
NC_000002.11:g.32353419T= , CM000664.1:g.32353419T=	GRCh37
NC_000002.10:g.32206923T=	NCBI36
NG_008730.1:g.69740T= , LRG_714:g.69740T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*834-58T=	ENSP00000515816.1:n.*834-58T=
ENST00000315285.9:c.1174-58T= MANE Select	ENSP00000320885.3:n.1174-58T=
ENST00000621856.2:c.1171-58T=	ENSP00000482496.2:n.1171-58T=
ENST00000642281.1:c.983-8213T=
ENST00000642455.1:c.1075-58T=	ENSP00000493827.1:n.1075-58T=
ENST00000642751.1:c.948-58T=
ENST00000642999.1:c.916-58T=	ENSP00000496589.1:n.916-58T=
ENST00000643327.1:c.333-58T=
ENST00000643334.1:c.754-58T=
ENST00000644408.1:c.1050-58T=
ENST00000644954.1:c.820-58T=	ENSP00000494312.1:n.820-58T=
ENST00000645159.1:n.1853T=
ENST00000645550.1:n.387-58T=
ENST00000645671.1:c.624-58T=
ENST00000645730.1:c.521-58T=
ENST00000646082.1:c.820-58T=
ENST00000646571.1:c.1078-58T=	ENSP00000495015.1:n.1078-58T=
ENST00000647007.1:n.866-58T=
ENST00000647133.1:c.674-58T=
ENST00000315285.7:c.1174-58T=	ENSP00000320885.3:n.1174-58T=
ENST00000345662.5:c.1078-58T=	ENSP00000340817.1:n.1078-58T=
ENST00000615843.4:c.1174-58T=	ENSP00000480893.1:n.1174-58T=
ENST00000621856.1:c.916-58T=	ENSP00000482496.1:n.916-58T=
NM_014946.3:c.1174-58T= , LRG_714t1:c.1174-58T=	NP_055761.2:n.1174-58T=
NM_199436.1:c.1078-58T=	NP_955468.1:n.1078-58T=
XM_005264516.3:c.1171-58T=	XP_005264573.1:n.1171-58T=
XM_011533067.1:c.1174-58T=	XP_011531369.1:n.1174-58T=
NM_001363823.1:c.1171-58T=	NP_001350752.1:n.1171-58T=
NM_001363875.1:c.1075-58T=	NP_001350804.1:n.1075-58T=
XM_005264516.5:c.1171-58T=	XP_005264573.1:n.1171-58T=
XM_011533067.2:c.1174-58T=	XP_011531369.1:n.1174-58T=
XM_017004778.2:c.1078-58T=	XP_016860267.1:n.1078-58T=
NM_001363823.2:c.1171-58T=	NP_001350752.1:n.1171-58T=
NM_001363875.2:c.1075-58T=	NP_001350804.1:n.1075-58T=
NM_001377959.1:c.1078-58T=	NP_001364888.1:n.1078-58T=
NM_014946.4:c.1174-58T= MANE Select	NP_055761.2:n.1174-58T=
NM_199436.2:c.1078-58T=	NP_955468.1:n.1078-58T=