Canonical Allele Identifier: CA1242477010

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32089451_32089452delinsTG , CM000664.2:g.32089451_32089452delinsTG	GRCh38
NC_000002.11:g.32314520_32314521delinsTG , CM000664.1:g.32314520_32314521delinsTG	GRCh37
NC_000002.10:g.32168024_32168025delinsTG	NCBI36
NG_008730.1:g.30841_30842delinsTG , LRG_714:g.30841_30842delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*163-71_*163-70delinsTG	ENSP00000515816.1:n.*163-71_*163-70delinsTG
ENST00000315285.9:c.503-71_503-70delinsTG MANE Select	ENSP00000320885.3:n.503-71_503-70delinsTG
ENST00000621856.2:c.500-71_500-70delinsTG	ENSP00000482496.2:n.500-71_500-70delinsTG
ENST00000642281.1:c.387-71_387-70delinsTG
ENST00000642455.1:c.500-71_500-70delinsTG	ENSP00000493827.1:n.500-71_500-70delinsTG
ENST00000642751.1:c.373-71_373-70delinsTG
ENST00000642999.1:c.245-71_245-70delinsTG	ENSP00000496589.1:n.245-71_245-70delinsTG
ENST00000643334.1:c.88-71_88-70delinsTG
ENST00000644408.1:c.379-71_379-70delinsTG
ENST00000644954.1:c.245-71_245-70delinsTG	ENSP00000494312.1:n.245-71_245-70delinsTG
ENST00000645400.1:c.459-71_459-70delinsTG	ENSP00000496306.1:n.459-71_459-70delinsTG
ENST00000645671.1:c.37-9345_37-9344delinsTG
ENST00000646082.1:c.337-71_337-70delinsTG
ENST00000646571.1:c.503-71_503-70delinsTG	ENSP00000495015.1:n.503-71_503-70delinsTG
ENST00000647007.1:n.200-71_200-70delinsTG
ENST00000647133.1:c.78-71_78-70delinsTG
ENST00000315285.7:c.503-71_503-70delinsTG	ENSP00000320885.3:n.503-71_503-70delinsTG
ENST00000345662.5:c.503-71_503-70delinsTG	ENSP00000340817.1:n.503-71_503-70delinsTG
ENST00000615843.4:c.503-71_503-70delinsTG	ENSP00000480893.1:n.503-71_503-70delinsTG
ENST00000621856.1:c.245-71_245-70delinsTG	ENSP00000482496.1:n.245-71_245-70delinsTG
NM_014946.3:c.503-71_503-70delinsTG , LRG_714t1:c.503-71_503-70delinsTG	NP_055761.2:n.503-71_503-70delinsTG
NM_199436.1:c.503-71_503-70delinsTG	NP_955468.1:n.503-71_503-70delinsTG
XM_005264516.3:c.500-71_500-70delinsTG	XP_005264573.1:n.500-71_500-70delinsTG
XM_011533067.1:c.503-71_503-70delinsTG	XP_011531369.1:n.503-71_503-70delinsTG
NM_001363823.1:c.500-71_500-70delinsTG	NP_001350752.1:n.500-71_500-70delinsTG
NM_001363875.1:c.500-71_500-70delinsTG	NP_001350804.1:n.500-71_500-70delinsTG
XM_005264516.5:c.500-71_500-70delinsTG	XP_005264573.1:n.500-71_500-70delinsTG
XM_011533067.2:c.503-71_503-70delinsTG	XP_011531369.1:n.503-71_503-70delinsTG
XM_017004778.2:c.503-71_503-70delinsTG	XP_016860267.1:n.503-71_503-70delinsTG
NM_001363823.2:c.500-71_500-70delinsTG	NP_001350752.1:n.500-71_500-70delinsTG
NM_001363875.2:c.500-71_500-70delinsTG	NP_001350804.1:n.500-71_500-70delinsTG
NM_001377959.1:c.503-71_503-70delinsTG	NP_001364888.1:n.503-71_503-70delinsTG
NM_014946.4:c.503-71_503-70delinsTG MANE Select	NP_055761.2:n.503-71_503-70delinsTG
NM_199436.2:c.503-71_503-70delinsTG	NP_955468.1:n.503-71_503-70delinsTG