Canonical Allele Identifier: CA1242498112

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128406_32128407delinsAG , CM000664.2:g.32128406_32128407delinsAG	GRCh38
NC_000002.11:g.32353475_32353476delinsAG , CM000664.1:g.32353475_32353476delinsAG	GRCh37
NC_000002.10:g.32206979_32206980delinsAG	NCBI36
NG_008730.1:g.69796_69797delinsAG , LRG_714:g.69796_69797delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*834-2_*834-1delinsAG	ENSP00000515816.1:n.*834-2_*834-1delinsAG
ENST00000315285.9:c.1174-2_1174-1delinsAG MANE Select	ENSP00000320885.3:n.1174-2_1174-1delinsAG
ENST00000621856.2:c.1171-2_1171-1delinsAG	ENSP00000482496.2:n.1171-2_1171-1delinsAG
ENST00000642281.1:c.983-8157_983-8156delinsAG
ENST00000642455.1:c.1075-2_1075-1delinsAG	ENSP00000493827.1:n.1075-2_1075-1delinsAG
ENST00000642751.1:c.948-2_948-1delinsAG
ENST00000642999.1:c.916-2_916-1delinsAG	ENSP00000496589.1:n.916-2_916-1delinsAG
ENST00000643327.1:c.333-2_333-1delinsAG
ENST00000643334.1:c.754-2_754-1delinsAG
ENST00000644408.1:c.1050-2_1050-1delinsAG
ENST00000644954.1:c.820-2_820-1delinsAG	ENSP00000494312.1:n.820-2_820-1delinsAG
ENST00000645159.1:n.1909_1910delinsAG
ENST00000645550.1:n.387-2_387-1delinsAG
ENST00000645671.1:c.624-2_624-1delinsAG
ENST00000645730.1:c.521-2_521-1delinsAG
ENST00000646082.1:c.820-2_820-1delinsAG
ENST00000646571.1:c.1078-2_1078-1delinsAG	ENSP00000495015.1:n.1078-2_1078-1delinsAG
ENST00000647007.1:n.866-2_866-1delinsAG
ENST00000647133.1:c.674-2_674-1delinsAG
ENST00000315285.7:c.1174-2_1174-1delinsAG	ENSP00000320885.3:n.1174-2_1174-1delinsAG
ENST00000345662.5:c.1078-2_1078-1delinsAG	ENSP00000340817.1:n.1078-2_1078-1delinsAG
ENST00000615843.4:c.1174-2_1174-1delinsAG	ENSP00000480893.1:n.1174-2_1174-1delinsAG
ENST00000621856.1:c.916-2_916-1delinsAG	ENSP00000482496.1:n.916-2_916-1delinsAG
NM_014946.3:c.1174-2_1174-1delinsAG , LRG_714t1:c.1174-2_1174-1delinsAG	NP_055761.2:n.1174-2_1174-1delinsAG
NM_199436.1:c.1078-2_1078-1delinsAG	NP_955468.1:n.1078-2_1078-1delinsAG
XM_005264516.3:c.1171-2_1171-1delinsAG	XP_005264573.1:n.1171-2_1171-1delinsAG
XM_011533067.1:c.1174-2_1174-1delinsAG	XP_011531369.1:n.1174-2_1174-1delinsAG
NM_001363823.1:c.1171-2_1171-1delinsAG	NP_001350752.1:n.1171-2_1171-1delinsAG
NM_001363875.1:c.1075-2_1075-1delinsAG	NP_001350804.1:n.1075-2_1075-1delinsAG
XM_005264516.5:c.1171-2_1171-1delinsAG	XP_005264573.1:n.1171-2_1171-1delinsAG
XM_011533067.2:c.1174-2_1174-1delinsAG	XP_011531369.1:n.1174-2_1174-1delinsAG
XM_017004778.2:c.1078-2_1078-1delinsAG	XP_016860267.1:n.1078-2_1078-1delinsAG
NM_001363823.2:c.1171-2_1171-1delinsAG	NP_001350752.1:n.1171-2_1171-1delinsAG
NM_001363875.2:c.1075-2_1075-1delinsAG	NP_001350804.1:n.1075-2_1075-1delinsAG
NM_001377959.1:c.1078-2_1078-1delinsAG	NP_001364888.1:n.1078-2_1078-1delinsAG
NM_014946.4:c.1174-2_1174-1delinsAG MANE Select	NP_055761.2:n.1174-2_1174-1delinsAG
NM_199436.2:c.1078-2_1078-1delinsAG	NP_955468.1:n.1078-2_1078-1delinsAG