Canonical Allele Identifier: CA2658527452

Gene: SPAST

Linked Data

• gnomAD v4: 2-32128348-GTTATCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128352_32128358del , CM000664.2:g.32128352_32128358del	GRCh38
NC_000002.11:g.32353421_32353427del , CM000664.1:g.32353421_32353427del	GRCh37
NC_000002.10:g.32206925_32206931del	NCBI36
NG_008730.1:g.69742_69748del , LRG_714:g.69742_69748del

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*834-56_*834-50del	ENSP00000515816.1:n.*834-56_*834-50del
ENST00000315285.9:c.1174-56_1174-50del MANE Select	ENSP00000320885.3:n.1174-56_1174-50del
ENST00000621856.2:c.1171-56_1171-50del	ENSP00000482496.2:n.1171-56_1171-50del
ENST00000642281.1:c.983-8211_983-8205del
ENST00000642455.1:c.1075-56_1075-50del	ENSP00000493827.1:n.1075-56_1075-50del
ENST00000642751.1:c.948-56_948-50del
ENST00000642999.1:c.916-56_916-50del	ENSP00000496589.1:n.916-56_916-50del
ENST00000643327.1:c.333-56_333-50del
ENST00000643334.1:c.754-56_754-50del
ENST00000644408.1:c.1050-56_1050-50del
ENST00000644954.1:c.820-56_820-50del	ENSP00000494312.1:n.820-56_820-50del
ENST00000645159.1:n.1855_1861del
ENST00000645550.1:n.387-56_387-50del
ENST00000645671.1:c.624-56_624-50del
ENST00000645730.1:c.521-56_521-50del
ENST00000646082.1:c.820-56_820-50del
ENST00000646571.1:c.1078-56_1078-50del	ENSP00000495015.1:n.1078-56_1078-50del
ENST00000647007.1:n.866-56_866-50del
ENST00000647133.1:c.674-56_674-50del
ENST00000315285.7:c.1174-56_1174-50del	ENSP00000320885.3:n.1174-56_1174-50del
ENST00000345662.5:c.1078-56_1078-50del	ENSP00000340817.1:n.1078-56_1078-50del
ENST00000615843.4:c.1174-56_1174-50del	ENSP00000480893.1:n.1174-56_1174-50del
ENST00000621856.1:c.916-56_916-50del	ENSP00000482496.1:n.916-56_916-50del
NM_014946.3:c.1174-56_1174-50del , LRG_714t1:c.1174-56_1174-50del	NP_055761.2:n.1174-56_1174-50del
NM_199436.1:c.1078-56_1078-50del	NP_955468.1:n.1078-56_1078-50del
XM_005264516.3:c.1171-56_1171-50del	XP_005264573.1:n.1171-56_1171-50del
XM_011533067.1:c.1174-56_1174-50del	XP_011531369.1:n.1174-56_1174-50del
NM_001363823.1:c.1171-56_1171-50del	NP_001350752.1:n.1171-56_1171-50del
NM_001363875.1:c.1075-56_1075-50del	NP_001350804.1:n.1075-56_1075-50del
XM_005264516.5:c.1171-56_1171-50del	XP_005264573.1:n.1171-56_1171-50del
XM_011533067.2:c.1174-56_1174-50del	XP_011531369.1:n.1174-56_1174-50del
XM_017004778.2:c.1078-56_1078-50del	XP_016860267.1:n.1078-56_1078-50del
NM_001363823.2:c.1171-56_1171-50del	NP_001350752.1:n.1171-56_1171-50del
NM_001363875.2:c.1075-56_1075-50del	NP_001350804.1:n.1075-56_1075-50del
NM_001377959.1:c.1078-56_1078-50del	NP_001364888.1:n.1078-56_1078-50del
NM_014946.4:c.1174-56_1174-50del MANE Select	NP_055761.2:n.1174-56_1174-50del
NM_199436.2:c.1078-56_1078-50del	NP_955468.1:n.1078-56_1078-50del