Canonical Allele Identifier: CA44742630

Gene: SPAST

Linked Data

• dbSNP Id: rs386644538

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128254_32128255delinsAC , CM000664.2:g.32128254_32128255delinsAC	GRCh38
NC_000002.11:g.32353323_32353324delinsAC , CM000664.1:g.32353323_32353324delinsAC	GRCh37
NC_000002.10:g.32206827_32206828delinsAC	NCBI36
NG_008730.1:g.69644_69645delinsAC , LRG_714:g.69644_69645delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*834-154_*834-153delinsAC	ENSP00000515816.1:n.*834-154_*834-153delinsAC
ENST00000315285.9:c.1174-154_1174-153delinsAC MANE Select	ENSP00000320885.3:n.1174-154_1174-153delinsAC
ENST00000621856.2:c.1171-154_1171-153delinsAC	ENSP00000482496.2:n.1171-154_1171-153delinsAC
ENST00000642281.1:c.983-8309_983-8308delinsAC
ENST00000642455.1:c.1075-154_1075-153delinsAC	ENSP00000493827.1:n.1075-154_1075-153delinsAC
ENST00000642751.1:c.948-154_948-153delinsAC
ENST00000642999.1:c.916-154_916-153delinsAC	ENSP00000496589.1:n.916-154_916-153delinsAC
ENST00000643327.1:c.333-154_333-153delinsAC
ENST00000643334.1:c.754-154_754-153delinsAC
ENST00000644408.1:c.1050-154_1050-153delinsAC
ENST00000644954.1:c.820-154_820-153delinsAC	ENSP00000494312.1:n.820-154_820-153delinsAC
ENST00000645159.1:n.1757_1758delinsAC
ENST00000645550.1:n.387-154_387-153delinsAC
ENST00000645671.1:c.624-154_624-153delinsAC
ENST00000645730.1:c.521-154_521-153delinsAC
ENST00000646082.1:c.820-154_820-153delinsAC
ENST00000646571.1:c.1078-154_1078-153delinsAC	ENSP00000495015.1:n.1078-154_1078-153delinsAC
ENST00000647007.1:n.866-154_866-153delinsAC
ENST00000647133.1:c.674-154_674-153delinsAC
ENST00000315285.7:c.1174-154_1174-153delinsAC	ENSP00000320885.3:n.1174-154_1174-153delinsAC
ENST00000345662.5:c.1078-154_1078-153delinsAC	ENSP00000340817.1:n.1078-154_1078-153delinsAC
ENST00000615843.4:c.1174-154_1174-153delinsAC	ENSP00000480893.1:n.1174-154_1174-153delinsAC
ENST00000621856.1:c.916-154_916-153delinsAC	ENSP00000482496.1:n.916-154_916-153delinsAC
NM_014946.3:c.1174-154_1174-153delinsAC , LRG_714t1:c.1174-154_1174-153delinsAC	NP_055761.2:n.1174-154_1174-153delinsAC
NM_199436.1:c.1078-154_1078-153delinsAC	NP_955468.1:n.1078-154_1078-153delinsAC
XM_005264516.3:c.1171-154_1171-153delinsAC	XP_005264573.1:n.1171-154_1171-153delinsAC
XM_011533067.1:c.1174-154_1174-153delinsAC	XP_011531369.1:n.1174-154_1174-153delinsAC
NM_001363823.1:c.1171-154_1171-153delinsAC	NP_001350752.1:n.1171-154_1171-153delinsAC
NM_001363875.1:c.1075-154_1075-153delinsAC	NP_001350804.1:n.1075-154_1075-153delinsAC
XM_005264516.5:c.1171-154_1171-153delinsAC	XP_005264573.1:n.1171-154_1171-153delinsAC
XM_011533067.2:c.1174-154_1174-153delinsAC	XP_011531369.1:n.1174-154_1174-153delinsAC
XM_017004778.2:c.1078-154_1078-153delinsAC	XP_016860267.1:n.1078-154_1078-153delinsAC
NM_001363823.2:c.1171-154_1171-153delinsAC	NP_001350752.1:n.1171-154_1171-153delinsAC
NM_001363875.2:c.1075-154_1075-153delinsAC	NP_001350804.1:n.1075-154_1075-153delinsAC
NM_001377959.1:c.1078-154_1078-153delinsAC	NP_001364888.1:n.1078-154_1078-153delinsAC
NM_014946.4:c.1174-154_1174-153delinsAC MANE Select	NP_055761.2:n.1174-154_1174-153delinsAC
NM_199436.2:c.1078-154_1078-153delinsAC	NP_955468.1:n.1078-154_1078-153delinsAC