Canonical Allele Identifier: CA2658527482

Gene: SPAST

Linked Data

• gnomAD v4: 2-32128392-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128393_32128394del , CM000664.2:g.32128393_32128394del	GRCh38
NC_000002.11:g.32353462_32353463del , CM000664.1:g.32353462_32353463del	GRCh37
NC_000002.10:g.32206966_32206967del	NCBI36
NG_008730.1:g.69783_69784del , LRG_714:g.69783_69784del

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*834-15_*834-14del	ENSP00000515816.1:n.*834-15_*834-14del
ENST00000315285.9:c.1174-15_1174-14del MANE Select	ENSP00000320885.3:n.1174-15_1174-14del
ENST00000621856.2:c.1171-15_1171-14del	ENSP00000482496.2:n.1171-15_1171-14del
ENST00000642281.1:c.983-8170_983-8169del
ENST00000642455.1:c.1075-15_1075-14del	ENSP00000493827.1:n.1075-15_1075-14del
ENST00000642751.1:c.948-15_948-14del
ENST00000642999.1:c.916-15_916-14del	ENSP00000496589.1:n.916-15_916-14del
ENST00000643327.1:c.333-15_333-14del
ENST00000643334.1:c.754-15_754-14del
ENST00000644408.1:c.1050-15_1050-14del
ENST00000644954.1:c.820-15_820-14del	ENSP00000494312.1:n.820-15_820-14del
ENST00000645159.1:n.1896_1897del
ENST00000645550.1:n.387-15_387-14del
ENST00000645671.1:c.624-15_624-14del
ENST00000645730.1:c.521-15_521-14del
ENST00000646082.1:c.820-15_820-14del
ENST00000646571.1:c.1078-15_1078-14del	ENSP00000495015.1:n.1078-15_1078-14del
ENST00000647007.1:n.866-15_866-14del
ENST00000647133.1:c.674-15_674-14del
ENST00000315285.7:c.1174-15_1174-14del	ENSP00000320885.3:n.1174-15_1174-14del
ENST00000345662.5:c.1078-15_1078-14del	ENSP00000340817.1:n.1078-15_1078-14del
ENST00000615843.4:c.1174-15_1174-14del	ENSP00000480893.1:n.1174-15_1174-14del
ENST00000621856.1:c.916-15_916-14del	ENSP00000482496.1:n.916-15_916-14del
NM_014946.3:c.1174-15_1174-14del , LRG_714t1:c.1174-15_1174-14del	NP_055761.2:n.1174-15_1174-14del
NM_199436.1:c.1078-15_1078-14del	NP_955468.1:n.1078-15_1078-14del
XM_005264516.3:c.1171-15_1171-14del	XP_005264573.1:n.1171-15_1171-14del
XM_011533067.1:c.1174-15_1174-14del	XP_011531369.1:n.1174-15_1174-14del
NM_001363823.1:c.1171-15_1171-14del	NP_001350752.1:n.1171-15_1171-14del
NM_001363875.1:c.1075-15_1075-14del	NP_001350804.1:n.1075-15_1075-14del
XM_005264516.5:c.1171-15_1171-14del	XP_005264573.1:n.1171-15_1171-14del
XM_011533067.2:c.1174-15_1174-14del	XP_011531369.1:n.1174-15_1174-14del
XM_017004778.2:c.1078-15_1078-14del	XP_016860267.1:n.1078-15_1078-14del
NM_001363823.2:c.1171-15_1171-14del	NP_001350752.1:n.1171-15_1171-14del
NM_001363875.2:c.1075-15_1075-14del	NP_001350804.1:n.1075-15_1075-14del
NM_001377959.1:c.1078-15_1078-14del	NP_001364888.1:n.1078-15_1078-14del
NM_014946.4:c.1174-15_1174-14del MANE Select	NP_055761.2:n.1174-15_1174-14del
NM_199436.2:c.1078-15_1078-14del	NP_955468.1:n.1078-15_1078-14del