Canonical Allele Identifier: CA1242498110

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128396_32128397delinsTG , CM000664.2:g.32128396_32128397delinsTG	GRCh38
NC_000002.11:g.32353465_32353466delinsTG , CM000664.1:g.32353465_32353466delinsTG	GRCh37
NC_000002.10:g.32206969_32206970delinsTG	NCBI36
NG_008730.1:g.69786_69787delinsTG , LRG_714:g.69786_69787delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*834-12_*834-11delinsTG	ENSP00000515816.1:n.*834-12_*834-11delinsTG
ENST00000315285.9:c.1174-12_1174-11delinsTG MANE Select	ENSP00000320885.3:n.1174-12_1174-11delinsTG
ENST00000621856.2:c.1171-12_1171-11delinsTG	ENSP00000482496.2:n.1171-12_1171-11delinsTG
ENST00000642281.1:c.983-8167_983-8166delinsTG
ENST00000642455.1:c.1075-12_1075-11delinsTG	ENSP00000493827.1:n.1075-12_1075-11delinsTG
ENST00000642751.1:c.948-12_948-11delinsTG
ENST00000642999.1:c.916-12_916-11delinsTG	ENSP00000496589.1:n.916-12_916-11delinsTG
ENST00000643327.1:c.333-12_333-11delinsTG
ENST00000643334.1:c.754-12_754-11delinsTG
ENST00000644408.1:c.1050-12_1050-11delinsTG
ENST00000644954.1:c.820-12_820-11delinsTG	ENSP00000494312.1:n.820-12_820-11delinsTG
ENST00000645159.1:n.1899_1900delinsTG
ENST00000645550.1:n.387-12_387-11delinsTG
ENST00000645671.1:c.624-12_624-11delinsTG
ENST00000645730.1:c.521-12_521-11delinsTG
ENST00000646082.1:c.820-12_820-11delinsTG
ENST00000646571.1:c.1078-12_1078-11delinsTG	ENSP00000495015.1:n.1078-12_1078-11delinsTG
ENST00000647007.1:n.866-12_866-11delinsTG
ENST00000647133.1:c.674-12_674-11delinsTG
ENST00000315285.7:c.1174-12_1174-11delinsTG	ENSP00000320885.3:n.1174-12_1174-11delinsTG
ENST00000345662.5:c.1078-12_1078-11delinsTG	ENSP00000340817.1:n.1078-12_1078-11delinsTG
ENST00000615843.4:c.1174-12_1174-11delinsTG	ENSP00000480893.1:n.1174-12_1174-11delinsTG
ENST00000621856.1:c.916-12_916-11delinsTG	ENSP00000482496.1:n.916-12_916-11delinsTG
NM_014946.3:c.1174-12_1174-11delinsTG , LRG_714t1:c.1174-12_1174-11delinsTG	NP_055761.2:n.1174-12_1174-11delinsTG
NM_199436.1:c.1078-12_1078-11delinsTG	NP_955468.1:n.1078-12_1078-11delinsTG
XM_005264516.3:c.1171-12_1171-11delinsTG	XP_005264573.1:n.1171-12_1171-11delinsTG
XM_011533067.1:c.1174-12_1174-11delinsTG	XP_011531369.1:n.1174-12_1174-11delinsTG
NM_001363823.1:c.1171-12_1171-11delinsTG	NP_001350752.1:n.1171-12_1171-11delinsTG
NM_001363875.1:c.1075-12_1075-11delinsTG	NP_001350804.1:n.1075-12_1075-11delinsTG
XM_005264516.5:c.1171-12_1171-11delinsTG	XP_005264573.1:n.1171-12_1171-11delinsTG
XM_011533067.2:c.1174-12_1174-11delinsTG	XP_011531369.1:n.1174-12_1174-11delinsTG
XM_017004778.2:c.1078-12_1078-11delinsTG	XP_016860267.1:n.1078-12_1078-11delinsTG
NM_001363823.2:c.1171-12_1171-11delinsTG	NP_001350752.1:n.1171-12_1171-11delinsTG
NM_001363875.2:c.1075-12_1075-11delinsTG	NP_001350804.1:n.1075-12_1075-11delinsTG
NM_001377959.1:c.1078-12_1078-11delinsTG	NP_001364888.1:n.1078-12_1078-11delinsTG
NM_014946.4:c.1174-12_1174-11delinsTG MANE Select	NP_055761.2:n.1174-12_1174-11delinsTG
NM_199436.2:c.1078-12_1078-11delinsTG	NP_955468.1:n.1078-12_1078-11delinsTG