Canonical Allele Identifier: CA1242498159

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128486_32128488delinsGCT , CM000664.2:g.32128486_32128488delinsGCT	GRCh38
NC_000002.11:g.32353555_32353557delinsGCT , CM000664.1:g.32353555_32353557delinsGCT	GRCh37
NC_000002.10:g.32207059_32207061delinsGCT	NCBI36
NG_008730.1:g.69876_69878delinsGCT , LRG_714:g.69876_69878delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*905+7_*905+9delinsGCT	ENSP00000515816.1:n.*905+7_*905+9delinsGCT
ENST00000315285.9:c.1245+7_1245+9delinsGCT MANE Select	ENSP00000320885.3:n.1245+7_1245+9delinsGCT
ENST00000621856.2:c.1242+7_1242+9delinsGCT	ENSP00000482496.2:n.1242+7_1242+9delinsGCT
ENST00000642281.1:c.983-8077_983-8075delinsGCT
ENST00000642455.1:c.1146+7_1146+9delinsGCT	ENSP00000493827.1:n.1146+7_1146+9delinsGCT
ENST00000642751.1:c.1019+7_1019+9delinsGCT
ENST00000642999.1:c.987+7_987+9delinsGCT	ENSP00000496589.1:n.987+7_987+9delinsGCT
ENST00000643327.1:c.404+7_404+9delinsGCT
ENST00000643334.1:c.825+7_825+9delinsGCT
ENST00000644408.1:c.1121+7_1121+9delinsGCT
ENST00000644954.1:c.891+7_891+9delinsGCT	ENSP00000494312.1:n.891+7_891+9delinsGCT
ENST00000645159.1:n.1982+7_1982+9delinsGCT
ENST00000645550.1:n.465_467delinsGCT
ENST00000645671.1:c.695+7_695+9delinsGCT
ENST00000645730.1:c.592+7_592+9delinsGCT
ENST00000646082.1:c.891+7_891+9delinsGCT
ENST00000646571.1:c.1149+7_1149+9delinsGCT	ENSP00000495015.1:n.1149+7_1149+9delinsGCT
ENST00000647007.1:n.937+7_937+9delinsGCT
ENST00000647133.1:c.745+7_745+9delinsGCT
ENST00000315285.7:c.1245+7_1245+9delinsGCT	ENSP00000320885.3:n.1245+7_1245+9delinsGCT
ENST00000345662.5:c.1149+7_1149+9delinsGCT	ENSP00000340817.1:n.1149+7_1149+9delinsGCT
ENST00000615843.4:c.1245+7_1245+9delinsGCT	ENSP00000480893.1:n.1245+7_1245+9delinsGCT
ENST00000621856.1:c.987+7_987+9delinsGCT	ENSP00000482496.1:n.987+7_987+9delinsGCT
NM_014946.3:c.1245+7_1245+9delinsGCT , LRG_714t1:c.1245+7_1245+9delinsGCT	NP_055761.2:n.1245+7_1245+9delinsGCT
NM_199436.1:c.1149+7_1149+9delinsGCT	NP_955468.1:n.1149+7_1149+9delinsGCT
XM_005264516.3:c.1242+7_1242+9delinsGCT	XP_005264573.1:n.1242+7_1242+9delinsGCT
XM_011533067.1:c.1245+7_1245+9delinsGCT	XP_011531369.1:n.1245+7_1245+9delinsGCT
NM_001363823.1:c.1242+7_1242+9delinsGCT	NP_001350752.1:n.1242+7_1242+9delinsGCT
NM_001363875.1:c.1146+7_1146+9delinsGCT	NP_001350804.1:n.1146+7_1146+9delinsGCT
XM_005264516.5:c.1242+7_1242+9delinsGCT	XP_005264573.1:n.1242+7_1242+9delinsGCT
XM_011533067.2:c.1245+7_1245+9delinsGCT	XP_011531369.1:n.1245+7_1245+9delinsGCT
XM_017004778.2:c.1149+7_1149+9delinsGCT	XP_016860267.1:n.1149+7_1149+9delinsGCT
NM_001363823.2:c.1242+7_1242+9delinsGCT	NP_001350752.1:n.1242+7_1242+9delinsGCT
NM_001363875.2:c.1146+7_1146+9delinsGCT	NP_001350804.1:n.1146+7_1146+9delinsGCT
NM_001377959.1:c.1149+7_1149+9delinsGCT	NP_001364888.1:n.1149+7_1149+9delinsGCT
NM_014946.4:c.1245+7_1245+9delinsGCT MANE Select	NP_055761.2:n.1245+7_1245+9delinsGCT
NM_199436.2:c.1149+7_1149+9delinsGCT	NP_955468.1:n.1149+7_1149+9delinsGCT